ID

29008

Descripción

Study ID: 101468/249 Clinical Study ID: 101468/249 Study Title: A 12-Week, Double-Blind, Placebo Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00363857 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: N/A Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication: Restless Legs Syndrome; Restless Legs Syndrome (RLS)

Palabras clave

  1. 20/2/18 20/2/18 -
Titular de derechos de autor

GlaxoSmithKline (GSK)

Subido en

20 de febrero de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Clinical Study, Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS), Study ID: 101468/249, NCT00363857

RLS Demographics and Examination Procedure

Demography
Descripción

Demography

Alias
UMLS CUI-1
C0011298
Date of Birth
Descripción

Date of Birth

Tipo de datos

date

Alias
UMLS CUI [1]
C0421451
Gender
Descripción

Gender

Tipo de datos

text

Alias
UMLS CUI [1]
C0079399
Race
Descripción

Race

Tipo de datos

integer

Alias
UMLS CUI [1]
C0034510
'Other' race, please specify:
Descripción

If you answered the previous question with 'other', please specify:

Tipo de datos

text

Alias
UMLS CUI [1]
C0034510
Vital signs
Descripción

Vital signs

Alias
UMLS CUI-1
C0518766
Height (without shoes)
Descripción

Height

Tipo de datos

integer

Unidades de medida
  • cm / in
Alias
UMLS CUI [1]
C0005890
cm / in
Weight (without shoes)
Descripción

Weight

Tipo de datos

integer

Unidades de medida
  • kg / lbs
Alias
UMLS CUI [1]
C0005910
kg / lbs
Pulse (after 5 minutes sitting)
Descripción

Pulse

Tipo de datos

integer

Unidades de medida
  • beats/min
Alias
UMLS CUI [1]
C0232117
beats/min
Sitting Blood Pressure (after 5 minutes sitting), systolic / diastolic
Descripción

Sitting Blood Pressure

Tipo de datos

integer

Unidades de medida
  • mmHg
Alias
UMLS CUI [1]
C0580946
mmHg
Orthostatic vital signs
Descripción

Orthostatic vital signs

Alias
UMLS CUI-1
C0518766
Screening
Descripción

Screening

Tipo de datos

integer

Alias
UMLS CUI [1]
C0220908
Time Vitals taken
Descripción

Time

Tipo de datos

time

Alias
UMLS CUI [1]
C0040223
Blood Pressure systolic / diastolic
Descripción

Blood Pressure

Tipo de datos

integer

Unidades de medida
  • mmHg
Alias
UMLS CUI [1]
C0005823
mmHg
Pulse
Descripción

Pulse

Tipo de datos

integer

Unidades de medida
  • beats/min
Alias
UMLS CUI [1]
C0232117
beats/min
Electrocardiogram
Descripción

Electrocardiogram

Alias
UMLS CUI-1
C0430456
Date of ECG:
Descripción

Date of ECG

Tipo de datos

date

Alias
UMLS CUI [1]
C2826640
Were any clinically significant abnormalities detected?
Descripción

If ’Yes’, please record details on the Significant Medical/Surgical History and Physical Examination or Baseline Signs and Symptoms/SAE pages and repeat prior to baseline.

Tipo de datos

integer

Alias
UMLS CUI [1]
C0522055
Laboratory evaluation
Descripción

Laboratory evaluation

Alias
UMLS CUI-1
C0022885
Date of blood sample:
Descripción

Read the instructions on the Quest Diagnostics shipment document and dispatch the samples for analysis accordingly.

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0011008
Were any clinically significant abnormalities detected?
Descripción

If ’Yes’, please record details on the Significant Medical/Surgical History and Physical Examination or Baseline Signs and Symptoms/SAE pages and repeat prior to baseline.

Tipo de datos

text

Alias
UMLS CUI [1]
C1853129
Pregnancy Dipstick
Descripción

Pregnancy Dipstick

Alias
UMLS CUI-1
C0430056
Is the patient a female of child-bearing potential?
Descripción

If ’Yes’, please perform a pregnancy dipstick test and record result below.

Tipo de datos

text

Alias
UMLS CUI [1]
C1960468
Pregnancy Dipstick result
Descripción

If ’Positive’, please record details on the Significant Medical/Surgical History and Physical Examination and exclude the patient.

Tipo de datos

text

Alias
UMLS CUI [1]
C0430056

Similar models

RLS Demographics and Examination Procedure

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Demography
C0011298 (UMLS CUI-1)
Date of Birth
Item
Date of Birth
date
C0421451 (UMLS CUI [1])
Item
Gender
text
C0079399 (UMLS CUI [1])
Code List
Gender
CL Item
Male (M)
CL Item
Female (F)
Item
Race
integer
C0034510 (UMLS CUI [1])
Code List
Race
CL Item
White (1)
CL Item
Black (2)
CL Item
Oriental (3)
CL Item
Other (4)
Race
Item
'Other' race, please specify:
text
C0034510 (UMLS CUI [1])
Item Group
Vital signs
C0518766 (UMLS CUI-1)
Height
Item
Height (without shoes)
integer
C0005890 (UMLS CUI [1])
Weight
Item
Weight (without shoes)
integer
C0005910 (UMLS CUI [1])
Pulse
Item
Pulse (after 5 minutes sitting)
integer
C0232117 (UMLS CUI [1])
Sitting Blood Pressure
Item
Sitting Blood Pressure (after 5 minutes sitting), systolic / diastolic
integer
C0580946 (UMLS CUI [1])
Item Group
Orthostatic vital signs
C0518766 (UMLS CUI-1)
Item
Screening
integer
C0220908 (UMLS CUI [1])
Code List
Screening
CL Item
After 10 minutes semi-supine (1)
CL Item
After erect for 1 minute (2)
Time
Item
Time Vitals taken
time
C0040223 (UMLS CUI [1])
Blood Pressure
Item
Blood Pressure systolic / diastolic
integer
C0005823 (UMLS CUI [1])
Pulse
Item
Pulse
integer
C0232117 (UMLS CUI [1])
Item Group
Electrocardiogram
C0430456 (UMLS CUI-1)
Date of ECG
Item
Date of ECG:
date
C2826640 (UMLS CUI [1])
Item
Were any clinically significant abnormalities detected?
integer
C0522055 (UMLS CUI [1])
Code List
Were any clinically significant abnormalities detected?
CL Item
No (1)
CL Item
Yes (2)
Item Group
Laboratory evaluation
C0022885 (UMLS CUI-1)
Date of blood sample
Item
Date of blood sample:
date
C0005834 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Were any clinically significant abnormalities detected?
text
C1853129 (UMLS CUI [1])
Code List
Were any clinically significant abnormalities detected?
CL Item
No (N)
CL Item
Yes (Y)
Item Group
Pregnancy Dipstick
C0430056 (UMLS CUI-1)
Item
Is the patient a female of child-bearing potential?
text
C1960468 (UMLS CUI [1])
Code List
Is the patient a female of child-bearing potential?
CL Item
No (N)
CL Item
Yes (Y)
Item
Pregnancy Dipstick result
text
C0430056 (UMLS CUI [1])
Code List
Pregnancy Dipstick result
CL Item
Negative (NEG)
CL Item
Positive (POS)

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial