ID

27190

Description

Study ID: 101468/188 Clinical Study ID: SKF-101468/188 Study Title:A Study of the Maintained Efficacy and Safety of Ropinirole Versus Placebo in the Long Term Treatment of Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication: Parkinson Disease Module: Baseline

Keywords

  1. 11/3/17 11/3/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

November 3, 2017

DOI

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License

Creative Commons BY-NC 3.0

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GSK Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/188

Baseline

  1. StudyEvent: ODM
    1. Baseline
Inclusion/Exclusion Criteria
Description

Inclusion/Exclusion Criteria

Alias
UMLS CUI-1
C0013893
Patient has a total score ≥ 15 on the RLS Rating Scale at baseline.
Description

Please complete the following inclusion criteria. If any of the above questions have been answered ’No’ exclude the patient from the study and complete the Patient Continuation/Withdrawal page at the back of this book.

Data type

boolean

Alias
UMLS CUI [1,1]
C0681889
UMLS CUI [1,2]
C0035258
UMLS CUI [2]
C1512693
Signs of secondary RLS (e.g. renal failure (end-stage renal disease), iron deficient anemia) or pregnancy at baseline.
Description

Please complete the following exclusion criteria. If any of the above questions have been answered ’Yes’ exclude the patient from the study and complete the Patient Continuation/Withdrawal page at the back of this book.

Data type

boolean

Alias
UMLS CUI [1]
C1536279
UMLS CUI [2]
C0032961
UMLS CUI [3]
C0680251
Patient suffers from augmentation and/or end of dose rebound at baseline.
Description

Please complete the following exclusion criteria. If any of the above questions have been answered ’Yes’ exclude the patient from the study and complete the Patient Continuation/Withdrawal page at the back of this book.

Data type

boolean

Alias
UMLS CUI [1]
C0473305
UMLS CUI [2]
C0454417
UMLS CUI [3]
C0680251
Patient has clinically significant abnormal laboratory, ECG or physical examination findings not resolved by the time of the baseline examinations.
Description

Please complete the following exclusion criteria. If any of the above questions have been answered ’Yes’ exclude the patient from the study and complete the Patient Continuation/Withdrawal page at the back of this book.

Data type

boolean

Alias
UMLS CUI [1]
C0438215
UMLS CUI [2]
C0522055
UMLS CUI [3]
C0747585
UMLS CUI [4]
C0680251
Patient is taking any medication known to induce drowsiness, affect RLS or sleep (the minimum discontinuation period is generally 5 half lives or 7 consecutive nights medication free, prior to baseline, whichever is the longer period).
Description

Please complete the following exclusion criteria. If any of the above questions have been answered ’Yes’ exclude the patient from the study and complete the Patient Continuation/Withdrawal page at the back of this book.

Data type

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0013144
UMLS CUI [2]
C0680251
Patient has a diastolic blood pressure ≥ 110mmHg or ≤ 50mmHg OR systolic blood pressure ≥ 180mmHg or ≤ 90mmHg at baseline.
Description

Please complete the following exclusion criteria. If any of the above questions have been answered ’Yes’ exclude the patient from the study and complete the Patient Continuation/Withdrawal page at the back of this book.

Data type

boolean

Alias
UMLS CUI [1]
C0005823
UMLS CUI [2]
C0680251
Patient has participated in any clinical drug or device trial in the 3 months prior to the baseline visit.
Description

Please complete the following exclusion criteria. If any of the above questions have been answered ’Yes’ exclude the patient from the study and complete the Patient Continuation/Withdrawal page at the back of this book.

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0680251
Patient has withdrawal, introduction, or change in dose of hormone replacement therapy (HRT) and/or any drug known to substantially inhibit CYP1A2 (e.g., ciprofloxacin, cimetidine, (HRT)) or induce CYP1A2 (e.g. tobacco, omeprazole) within 7 days prior to enrolment. Patients already on these agents may be enrolled but must remain on stable doses of the agent from 7 days prior to enrolment through to the follow-up visit at end of study.
Description

Please complete the following exclusion criteria. If any of the above questions have been answered ’Yes’ exclude the patient from the study and complete the Patient Continuation/Withdrawal page at the back of this book.

Data type

boolean

Alias
UMLS CUI [1]
C0282402
UMLS CUI [2]
C0680251
RLS Rating Scales: Mark the patient’s total score for all 10 items
Description

Please complete the Baseline RLS Rating Scale from the RLS Rating Scale Book.If this score is not ≥ 15, exclude the patient

Data type

integer

Alias
UMLS CUI [1,1]
C0681889
UMLS CUI [1,2]
C0035258
UMLS CUI [1,3]
C0282121
Vital signs
Description

Vital signs

Alias
UMLS CUI-1
C0518766
UMLS CUI-2
C0031809
Sitting blood pressure systolic
Description

Sitting blood pressure systolic

Data type

integer

Measurement units
  • mmHg
Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0277814
mmHg
Sitting blood pressure diastolic
Description

Sitting blood pressure diastolic

Data type

integer

Measurement units
  • mmHg
Alias
UMLS CUI [1,1]
C0428883
UMLS CUI [1,2]
C0277814
mmHg
Sitting heart rate
Description

Sitting heart rate

Data type

integer

Measurement units
  • beats/min
Alias
UMLS CUI [1,1]
C0018810
UMLS CUI [1,2]
C0277814
beats/min
Baseline Employment Status
Description

Baseline Employment Status

Alias
UMLS CUI-1
C0242271
UMLS CUI-2
C1955348
Which of the following categories best describes the patient at this time?
Description

Employment status

Data type

integer

Alias
UMLS CUI [1]
C0242271
If part-time employed, please list approximate hours per week
Description

Part-time employment

Data type

float

Measurement units
  • hours/week
Alias
UMLS CUI [1,1]
C0682294
UMLS CUI [1,2]
C2584953
hours/week
If volunteer/unpaid work, please list approximate hours per week
Description

Volunteer/Unpaid work

Data type

float

Measurement units
  • hours/week
Alias
UMLS CUI [1,1]
C2367294
UMLS CUI [1,2]
C0557361
UMLS CUI [1,3]
C2584953
hours/week
If retired, please specify date of retirement
Description

Date of retirement

Data type

date

Alias
UMLS CUI [1,1]
C0035345
UMLS CUI [1,2]
C0011008
If patient is employed (full-time, part-time or an unpaid volunteer) or seeking work, please mark the one option below which best describes the category of the patient´s occupation:
Description

Patient´s occupation

Data type

integer

Alias
UMLS CUI [1]
C0421456
Healthcare resource utilisation - Visits/Contacts with Physicians
Description

Healthcare resource utilisation - Visits/Contacts with Physicians

Alias
UMLS CUI-1
C1704738
UMLS CUI-2
C0031831
UMLS CUI-3
C0545082
In the past 4 weeks...did the patient visit your site (for reasons other than study visit) or other medical practitioners?
Description

If ’No’, please leave the rest of this page blank If ’Yes’, please describe each visit

Data type

boolean

Alias
UMLS CUI [1]
C0583555
Date of Visit
Description

date of visit physician

Data type

date

Alias
UMLS CUI [1,1]
C1320303
UMLS CUI [1,2]
C0031831
Type of physician
Description

Type of physician

Data type

integer

Alias
UMLS CUI [1,1]
C0031831
UMLS CUI [1,2]
C0332307
Visit location
Description

Visit location

Data type

integer

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C0450429
Was the Visit RLS Related?
Description

A Directly Related RLS visit is one that in your opinion is specifically related to the patient's RLS (e.g. visits for RLS treatment, testing etc).

Data type

text

Alias
UMLS CUI [1,1]
C0035258
UMLS CUI [1,2]
C0439849
Were any tests or procedures prescribed or conducted at this visit?
Description

tests or procedures prescribed

Data type

integer

Alias
UMLS CUI [1]
C0430022
UMLS CUI [2]
C0033080
Healthcare resource utilisation - Visits/Contacts with other Paramedical Practitioners
Description

Healthcare resource utilisation - Visits/Contacts with other Paramedical Practitioners

Alias
UMLS CUI-1
C1704738
UMLS CUI-2
C0030450
UMLS CUI-3
C0545082
In the past 4 weeks...did the patient visit any or have contact with paramedical practitioners (for reasons other than study visit)?
Description

If ’No’, please leave the rest of this page blank If ’Yes’, please describe each visit

Data type

boolean

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C0030450
Date of visit
Description

date of visit paramedical practitioner

Data type

date

Alias
UMLS CUI [1,1]
C0030450
UMLS CUI [1,2]
C1320303
Type of paramedical practitioner
Description

Type of paramedical practitioner

Data type

integer

Alias
UMLS CUI [1,1]
C0030450
UMLS CUI [1,2]
C0332307
Visit location
Description

Visit location

Data type

integer

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C0450429
Was the visit RLS related?
Description

A Directly Related RLS visit is one that in your opinion is specifically related to the patient's RLS (e.g. visits for RLS treatment, testing etc).

Data type

text

Alias
UMLS CUI [1,1]
C0035258
UMLS CUI [1,2]
C0439849
Healthcare resource utilisation - Hospitalisation
Description

Healthcare resource utilisation - Hospitalisation

Alias
UMLS CUI-1
C1704738
UMLS CUI-2
C0019993
In the past 4 weeks...was the patient hospitalised?
Description

If ’No’, please leave the rest of this page blank If ’Yes’, please describe each hospitalisation

Data type

boolean

Alias
UMLS CUI [1]
C0019993
Date of admission
Description

date of admission

Data type

date

Alias
UMLS CUI [1]
C1302393
Date of discharge
Description

date of discharge

Data type

date

Alias
UMLS CUI [1]
C2361123
Main reason for stay
Description

Hospitalisation cause

Data type

text

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0392360
Was the Visit RLS Related?
Description

A Directly Related RLS visit is one that in your opinion is specifically related to the patient's RLS (e.g. visits for RLS treatment, testing etc). An Indirectly Related RLS visit is one that in your opinion is related to conditions or complications caused by the underlying RLS condition (e.g. visit to treat associated sleep disorders, etc). A Not Related RLS visit is one that in your opinion is related to other reasons.

Data type

text

Alias
UMLS CUI [1,1]
C0035258
UMLS CUI [1,2]
C0439849
Type of ward
Description

type of ward

Data type

integer

Alias
UMLS CUI [1,1]
C1305702
UMLS CUI [1,2]
C0332307
Length of stay on ward
Description

in days

Data type

integer

Measurement units
  • days
Alias
UMLS CUI [1,1]
C1305702
UMLS CUI [1,2]
C0023303
days
Healthcare resource utilisation - accident & emergency / emergency room visits
Description

Healthcare resource utilisation - accident & emergency / emergency room visits

Alias
UMLS CUI-1
C1704738
UMLS CUI-2
C0562508
UMLS CUI-3
C0545082
In the past 4 weeks...did the patient visit an Accident and Emergency or EMERGENCY ROOM?
Description

If ’No’, please leave the rest of this page blank If ’Yes’, please describe each visit

Data type

boolean

Alias
UMLS CUI [1,1]
C0562508
UMLS CUI [1,2]
C0545082
Date of visit
Description

Date of visit in A&E

Data type

date

Alias
UMLS CUI [1,1]
C0562508
UMLS CUI [1,2]
C1320303
Was the visit RLS related?
Description

A Directly Related RLS visit is one that in your opinion is specifically related to the patient's RLS (e.g. visits for RLS treatment, testing etc). An Indirectly Related RLS visit is one that in your opinion is related to conditions or complications caused by the underlying RLS condition (e.g. visit to treat associated sleep disorders, etc). A Not Related RLS visit is one that in your opinion is related to other reasons.

Data type

text

Alias
UMLS CUI [1,1]
C0035258
UMLS CUI [1,2]
C0439849

Similar models

Baseline

  1. StudyEvent: ODM
    1. Baseline
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion/Exclusion Criteria
C0013893 (UMLS CUI-1)
RLS Rating Scale
Item
Patient has a total score ≥ 15 on the RLS Rating Scale at baseline.
boolean
C0681889 (UMLS CUI [1,1])
C0035258 (UMLS CUI [1,2])
C1512693 (UMLS CUI [2])
secondary RLS or pregnancy
Item
Signs of secondary RLS (e.g. renal failure (end-stage renal disease), iron deficient anemia) or pregnancy at baseline.
boolean
C1536279 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
C0680251 (UMLS CUI [3])
augmentation and/or end of dose rebound
Item
Patient suffers from augmentation and/or end of dose rebound at baseline.
boolean
C0473305 (UMLS CUI [1])
C0454417 (UMLS CUI [2])
C0680251 (UMLS CUI [3])
clinically significant abnormal laboratory, ECG or physical examination findings
Item
Patient has clinically significant abnormal laboratory, ECG or physical examination findings not resolved by the time of the baseline examinations.
boolean
C0438215 (UMLS CUI [1])
C0522055 (UMLS CUI [2])
C0747585 (UMLS CUI [3])
C0680251 (UMLS CUI [4])
medication known to induce drowsiness, affect RLS or sleep
Item
Patient is taking any medication known to induce drowsiness, affect RLS or sleep (the minimum discontinuation period is generally 5 half lives or 7 consecutive nights medication free, prior to baseline, whichever is the longer period).
boolean
C0013227 (UMLS CUI [1,1])
C0013144 (UMLS CUI [1,2])
C0680251 (UMLS CUI [2])
blood pressure
Item
Patient has a diastolic blood pressure ≥ 110mmHg or ≤ 50mmHg OR systolic blood pressure ≥ 180mmHg or ≤ 90mmHg at baseline.
boolean
C0005823 (UMLS CUI [1])
C0680251 (UMLS CUI [2])
participated in any clinical drug or device trial
Item
Patient has participated in any clinical drug or device trial in the 3 months prior to the baseline visit.
boolean
C2348568 (UMLS CUI [1])
C0680251 (UMLS CUI [2])
hormone replacement therapy
Item
Patient has withdrawal, introduction, or change in dose of hormone replacement therapy (HRT) and/or any drug known to substantially inhibit CYP1A2 (e.g., ciprofloxacin, cimetidine, (HRT)) or induce CYP1A2 (e.g. tobacco, omeprazole) within 7 days prior to enrolment. Patients already on these agents may be enrolled but must remain on stable doses of the agent from 7 days prior to enrolment through to the follow-up visit at end of study.
boolean
C0282402 (UMLS CUI [1])
C0680251 (UMLS CUI [2])
Baseline RLS Score
Item
RLS Rating Scales: Mark the patient’s total score for all 10 items
integer
C0681889 (UMLS CUI [1,1])
C0035258 (UMLS CUI [1,2])
C0282121 (UMLS CUI [1,3])
Item Group
Vital signs
C0518766 (UMLS CUI-1)
C0031809 (UMLS CUI-2)
Sitting blood pressure systolic
Item
Sitting blood pressure systolic
integer
C0871470 (UMLS CUI [1,1])
C0277814 (UMLS CUI [1,2])
Sitting blood pressure diastolic
Item
Sitting blood pressure diastolic
integer
C0428883 (UMLS CUI [1,1])
C0277814 (UMLS CUI [1,2])
Sitting heart rate
Item
Sitting heart rate
integer
C0018810 (UMLS CUI [1,1])
C0277814 (UMLS CUI [1,2])
Item Group
Baseline Employment Status
C0242271 (UMLS CUI-1)
C1955348 (UMLS CUI-2)
Item
Which of the following categories best describes the patient at this time?
integer
C0242271 (UMLS CUI [1])
Code List
Which of the following categories best describes the patient at this time?
CL Item
Full time employment (1)
CL Item
Part-time employment  (2)
CL Item
Volunteer/Unpaid work  (3)
CL Item
Unemployed due to RLS (4)
CL Item
Unemployed due to other (non-RLS) disability (5)
CL Item
Unempoyed for other reason  (6)
CL Item
Retired  (7)
CL Item
Homemaker (8)
Part-time employment
Item
If part-time employed, please list approximate hours per week
float
C0682294 (UMLS CUI [1,1])
C2584953 (UMLS CUI [1,2])
Volunteer/Unpaid work
Item
If volunteer/unpaid work, please list approximate hours per week
float
C2367294 (UMLS CUI [1,1])
C0557361 (UMLS CUI [1,2])
C2584953 (UMLS CUI [1,3])
Date of retirement
Item
If retired, please specify date of retirement
date
C0035345 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
If patient is employed (full-time, part-time or an unpaid volunteer) or seeking work, please mark the one option below which best describes the category of the patient´s occupation:
integer
C0421456 (UMLS CUI [1])
Code List
If patient is employed (full-time, part-time or an unpaid volunteer) or seeking work, please mark the one option below which best describes the category of the patient´s occupation:
CL Item
Legislator, senior official or manager (e.g specialist managers, directors and chief executives) (1)
CL Item
Professional (e.g. teaching, legal, science and health professionals) (2)
CL Item
Technician or associate professional (computer associates, nurses/midwifes, ship & aircraft controllers, police inspectors, finance & sales) (3)
CL Item
Clerk (secretaries, cashiers and other office clerks) (4)
CL Item
Service worker or shop and market sales worker (e.g housekeeping and restaurant services, shop salesperson & demonstrators, and models) (5)
CL Item
Skilled agricultural or fishery worker (e.g animal/crop producers, market gardeners, fishery workers, hunters and trappers) (6)
CL Item
Craft and related trade workers (e.g miners, builders, blacksmiths, potters, glass-makers, textile workers) (7)
CL Item
Plant and machine operator or assembler (e.g. metal processing plant operator, food and related products machine operators) (8)
CL Item
Military (9)
Item Group
Healthcare resource utilisation - Visits/Contacts with Physicians
C1704738 (UMLS CUI-1)
C0031831 (UMLS CUI-2)
C0545082 (UMLS CUI-3)
Visits with physicians
Item
In the past 4 weeks...did the patient visit your site (for reasons other than study visit) or other medical practitioners?
boolean
C0583555 (UMLS CUI [1])
date of visit physician
Item
Date of Visit
date
C1320303 (UMLS CUI [1,1])
C0031831 (UMLS CUI [1,2])
Item
Type of physician
integer
C0031831 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Type of physician
CL Item
Cardiologist (1)
CL Item
Diabetologist (2)
CL Item
Dermatologist (3)
CL Item
Endocrinologist (4)
CL Item
ENT (Ear Nose & Throat) (5)
CL Item
Gastroenterologist (6)
CL Item
General/Internal Medical (7)
CL Item
General Practitioner/Family Practitioner  (8)
CL Item
Geriatrician (9)
CL Item
Gynaecologist (10)
CL Item
Infectious Disease (11)
CL Item
Nephrologist (12)
CL Item
Neurologist (13)
CL Item
Psychiatrist (14)
CL Item
Orthopaedic (15)
CL Item
Oncologist (16)
CL Item
Ophthalmologist (17)
CL Item
Respiratory/Chest Physician  (18)
CL Item
Rheumatologist (19)
CL Item
Urologist (20)
CL Item
Sleep Disorder Specialist  (21)
CL Item
Other (99)
Item
Visit location
integer
C0545082 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
Code List
Visit location
CL Item
Non hospital Office visit (eg GP surgery, Specialist's office etc) (1)
CL Item
Hospital Out Patient visit (2)
CL Item
At the Patient's home / domiciliary visit (3)
Item
Was the Visit RLS Related?
text
C0035258 (UMLS CUI [1,1])
C0439849 (UMLS CUI [1,2])
Code List
Was the Visit RLS Related?
CL Item
directly (1)
CL Item
indirectly (2)
CL Item
not related (3)
Item
Were any tests or procedures prescribed or conducted at this visit?
integer
C0430022 (UMLS CUI [1])
C0033080 (UMLS CUI [2])
Code List
Were any tests or procedures prescribed or conducted at this visit?
CL Item
yes (1)
CL Item
no (2)
CL Item
unknown (3)
Item Group
Healthcare resource utilisation - Visits/Contacts with other Paramedical Practitioners
C1704738 (UMLS CUI-1)
C0030450 (UMLS CUI-2)
C0545082 (UMLS CUI-3)
patient visit with paramedical practitioners
Item
In the past 4 weeks...did the patient visit any or have contact with paramedical practitioners (for reasons other than study visit)?
boolean
C0545082 (UMLS CUI [1,1])
C0030450 (UMLS CUI [1,2])
date of visit paramedical practitioner
Item
Date of visit
date
C0030450 (UMLS CUI [1,1])
C1320303 (UMLS CUI [1,2])
Item
Type of paramedical practitioner
integer
C0030450 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Type of paramedical practitioner
CL Item
Acupuncturist (1)
CL Item
Chiropodist/ Footcare Practitioner (2)
CL Item
Chiropractor (3)
CL Item
Dentist (4)
CL Item
Dietician (5)
CL Item
Homeopath/Herbalist (6)
CL Item
Nurse (7)
CL Item
Osteopath (8)
CL Item
Physiotherapist (9)
CL Item
Other (99)
Item
Visit location
integer
C0545082 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
Code List
Visit location
CL Item
Non hospital Office visit (eg GP surgery, Specialist's office etc) (1)
CL Item
Hospital Out Patient visit (2)
CL Item
At the Patient's home / domiciliary visit (3)
Item
Was the visit RLS related?
text
C0035258 (UMLS CUI [1,1])
C0439849 (UMLS CUI [1,2])
Code List
Was the visit RLS related?
CL Item
directly (1)
CL Item
indirectly (2)
CL Item
not related (3)
Item Group
Healthcare resource utilisation - Hospitalisation
C1704738 (UMLS CUI-1)
C0019993 (UMLS CUI-2)
Hospitalisation
Item
In the past 4 weeks...was the patient hospitalised?
boolean
C0019993 (UMLS CUI [1])
date of admission
Item
Date of admission
date
C1302393 (UMLS CUI [1])
date of discharge
Item
Date of discharge
date
C2361123 (UMLS CUI [1])
Hospitalisation cause
Item
Main reason for stay
text
C0019993 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Item
Was the Visit RLS Related?
text
C0035258 (UMLS CUI [1,1])
C0439849 (UMLS CUI [1,2])
Code List
Was the Visit RLS Related?
CL Item
directly (1)
CL Item
indirectly (2)
CL Item
not related (3)
Item
Type of ward
integer
C1305702 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Type of ward
CL Item
Cardiovascular (1)
CL Item
Dermatological (2)
CL Item
Endocrinological (3)
CL Item
ENT (Ear, Nose & Throat)  (4)
CL Item
Gastroenterological (5)
CL Item
General Medical (6)
CL Item
Geriatric (7)
CL Item
Gynaecological (8)
CL Item
Infectious Disease  (9)
CL Item
Nephrological (10)
CL Item
Intensive Care  (11)
CL Item
Neurological  (12)
CL Item
Psychiatric (13)
CL Item
Orthopaedic  (14)
CL Item
Oncology (15)
CL Item
Ophthalmological  (16)
CL Item
Respiratory/Chest  (17)
CL Item
Rheumatological  (18)
CL Item
Urological (19)
CL Item
Other (99)
length of stay on ward
Item
Length of stay on ward
integer
C1305702 (UMLS CUI [1,1])
C0023303 (UMLS CUI [1,2])
Item Group
Healthcare resource utilisation - accident & emergency / emergency room visits
C1704738 (UMLS CUI-1)
C0562508 (UMLS CUI-2)
C0545082 (UMLS CUI-3)
A&E visits
Item
In the past 4 weeks...did the patient visit an Accident and Emergency or EMERGENCY ROOM?
boolean
C0562508 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
Date of visit in A&E
Item
Date of visit
date
C0562508 (UMLS CUI [1,1])
C1320303 (UMLS CUI [1,2])
Item
Was the visit RLS related?
text
C0035258 (UMLS CUI [1,1])
C0439849 (UMLS CUI [1,2])
Code List
Was the visit RLS related?
CL Item
directly (1)
CL Item
indirectly (2)
CL Item
not related (3)

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