ID

18159

Beschrijving

Study Type: Interventional Study Design: Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment Official Title: Therapy for Chronic Cold Agglutinin Disease: A Prospective, Non-Randomized Multi-Center Study Demonstrating the Efficacy of Terminal Complement Inhibition in Patients With Cold Agglutinin Disease Using Eculizumab EudraCT-Nummer 2009-01696697 ClinicalTrials.gov-Identifier NCT01303952 https://clinicaltrials.gov/ct2/show/NCT01303952 Genehmigung durch Frau Ose

Link

https://clinicaltrials.gov/ct2/show/NCT01303952

Trefwoorden

  1. 18-10-16 18-10-16 -
  2. 21-10-16 21-10-16 -
  3. 24-10-16 24-10-16 -
Geüploaded op

24 oktober 2016

DOI

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Licentie

Creative Commons BY 4.0

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Induction Period - Visit 1 Observation Period UK Essen Therapy of Chronic Cold Agglutinin Disease With Eculizumab NCT01303952

Induction Period - Visit 1 Observation Period UK Essen Therapy of Chronic Cold Agglutinin Disease With Eculizumab NCT01303952

Date of Visit
Beschrijving

Date of Visit

Alias
UMLS CUI-1
C1320303
Date of Visit
Beschrijving

Date of Visit

Datatype

text

Maateenheden
  • YYYY-MM-DD
Alias
UMLS CUI [1]
C1320303
YYYY-MM-DD
Patient is eligible for study (All inclusion criteria apply and no exclusion criteria)
Beschrijving

eligibility

Datatype

integer

Alias
UMLS CUI [1]
C1302261
Was the study terminated prematurely?
Beschrijving

early termination

Datatype

integer

Alias
UMLS CUI [1]
C2718058
LDH
Beschrijving

LDH

Alias
UMLS CUI-1
C0202113
LDH
Beschrijving

Sub-Itemgroup: Demographics

Datatype

float

Maateenheden
  • U/l
Alias
UMLS CUI [1]
C0202113
U/l
Vital signs
Beschrijving

Vital signs

Alias
UMLS CUI-1
C0518766
1. Systolic blood pressure
Beschrijving

Sub-Itemgroup: Vital Signs

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI [1]
C0871470
mmHg
1. Diastolic blood pressure
Beschrijving

Sub-Itemgroup: Vital Signs

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI [1]
C0428883
mmHg
2. Systolic blood pressure
Beschrijving

Sub-Itemgroup: Vital Signs

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI [1]
C0871470
mmHg
2. Diastolic blood pressure
Beschrijving

Sub-Itemgroup: Vital Signs

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI [1]
C0428883
mmHg
3. Systolic blood pressure
Beschrijving

Sub-Itemgroup: Vital Signs

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI [1]
C0871470
mmHg
3. Diastolic blood pressure
Beschrijving

Sub-Itemgroup: Vital Signs

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI [1]
C0428883
mmHg
Sitting heart rate
Beschrijving

Sub-Itemgroup: Vital Signs

Datatype

integer

Maateenheden
  • beats per minute
Alias
UMLS CUI [1]
C2029904
beats per minute
Body temperature
Beschrijving

Sub-Itemgroup: Vital Signs

Datatype

float

Maateenheden
  • °C
Alias
UMLS CUI [1]
C0005903
°C
Six-Minute Walk Test
Beschrijving

Six-Minute Walk Test

Alias
UMLS CUI-1
C0430515
Walk distance
Beschrijving

Sub-Itemgroup: Six-Minute Walk Test

Datatype

integer

Maateenheden
  • Meter
Alias
UMLS CUI [1]
C3854161
Meter
Does the patient report symptoms of dyspnea?
Beschrijving

Sub-Itemgroup: Six-Minute Walk Test

Datatype

integer

Alias
UMLS CUI [1]
C0013404
Circulatory Symptoms
Beschrijving

Circulatory Symptoms

Alias
UMLS CUI-1
C0476270
Thrombophlebitis/Deep Vein Thrombosis
Beschrijving

Thrombophlebitis/Deep Vein Thrombosis

Datatype

integer

Alias
UMLS CUI [1]
C0040046
UMLS CUI [2]
C0149871
Pulmonary Embolus
Beschrijving

Pulmonary Embolus

Datatype

integer

Alias
UMLS CUI [1]
C0034065
Cerebrovascular Accident
Beschrijving

Cerebrovascular Accident

Datatype

integer

Alias
UMLS CUI [1]
C0038454
Amputation
Beschrijving

Amputation

Datatype

integer

Alias
UMLS CUI [1]
C0002688
Myocardial Infarction
Beschrijving

Myocardial Infarction

Datatype

integer

Alias
UMLS CUI [1]
C0027051
Transient Ischemic Attack
Beschrijving

Transient Ischemic Attack

Datatype

integer

Alias
UMLS CUI [1]
C0007787
Unstable Angina
Beschrijving

Unstable Angina

Datatype

integer

Alias
UMLS CUI [1]
C0002965
Renal Vein Thrombosis
Beschrijving

Renal Vein Thrombosis

Datatype

integer

Alias
UMLS CUI [1]
C0238457
Mesenteric Vein Thrombosis
Beschrijving

Mesenteric Vein Thrombosis

Datatype

integer

Alias
UMLS CUI [1]
C0267412
Portal Vein Thrombosis (Budd-Chiari)
Beschrijving

Portal Vein Thrombosis (Budd-Chiari)

Datatype

integer

Alias
UMLS CUI [1]
C0155773
Gangrene
Beschrijving

Gangrene

Datatype

integer

Alias
UMLS CUI [1]
C0017086
Acute Peripheral Vascular Occlusion
Beschrijving

Acute Peripheral Vascular Occlusion

Datatype

integer

Alias
UMLS CUI [1]
C0240728
Sudden Death
Beschrijving

Sudden Death

Datatype

integer

Alias
UMLS CUI [1]
C0011071
Patient suffers from other accompanying illnesses?
Beschrijving

Patient suffers from other accompanying illnesses?

Datatype

integer

Alias
UMLS CUI [1]
C0009488
Only for Woman (under 50): Is the pregnancy test negativ?
Beschrijving

Only for Woman (under 50): Is the pregnancy test negativ?

Datatype

integer

Alias
UMLS CUI [1]
C0032976
Comments
Beschrijving

Comments

Datatype

text

Alias
UMLS CUI [1]
C0947611
Signature principal investigator
Beschrijving

Signature principal investigator

Alias
UMLS CUI-1
C1519316
UMLS CUI-2
C1521895
Signature date
Beschrijving

Signature date

Datatype

text

Maateenheden
  • YYYY-MM-DD
Alias
UMLS CUI [1]
C0807937
YYYY-MM-DD
Signature investigator
Beschrijving

Signature investigator

Datatype

integer

Alias
UMLS CUI [1]
C2346576

Similar models

Induction Period - Visit 1 Observation Period UK Essen Therapy of Chronic Cold Agglutinin Disease With Eculizumab NCT01303952

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Date of Visit
C1320303 (UMLS CUI-1)
Date of Visit
Item
Date of Visit
text
C1320303 (UMLS CUI [1])
Item
Patient is eligible for study (All inclusion criteria apply and no exclusion criteria)
integer
C1302261 (UMLS CUI [1])
Code List
Patient is eligible for study (All inclusion criteria apply and no exclusion criteria)
CL Item
no (0)
CL Item
yes (1)
Item
Was the study terminated prematurely?
integer
C2718058 (UMLS CUI [1])
Code List
Was the study terminated prematurely?
CL Item
no (0)
CL Item
yes (1)
Item Group
LDH
C0202113 (UMLS CUI-1)
LDH
Item
LDH
float
C0202113 (UMLS CUI [1])
Item Group
Vital signs
C0518766 (UMLS CUI-1)
1. Systolic blood pressure
Item
1. Systolic blood pressure
integer
C0871470 (UMLS CUI [1])
1. Diastolic blood pressure
Item
1. Diastolic blood pressure
integer
C0428883 (UMLS CUI [1])
2. Systolic blood pressure
Item
2. Systolic blood pressure
integer
C0871470 (UMLS CUI [1])
2. Diastolic blood pressure
Item
2. Diastolic blood pressure
integer
C0428883 (UMLS CUI [1])
3. Systolic blood pressure
Item
3. Systolic blood pressure
integer
C0871470 (UMLS CUI [1])
3. Diastolic blood pressure
Item
3. Diastolic blood pressure
integer
C0428883 (UMLS CUI [1])
Sitting heart rate
Item
Sitting heart rate
integer
C2029904 (UMLS CUI [1])
Body temperature
Item
Body temperature
float
C0005903 (UMLS CUI [1])
Item Group
Six-Minute Walk Test
C0430515 (UMLS CUI-1)
Walk distance
Item
Walk distance
integer
C3854161 (UMLS CUI [1])
Item
Does the patient report symptoms of dyspnea?
integer
C0013404 (UMLS CUI [1])
Code List
Does the patient report symptoms of dyspnea?
CL Item
no (0)
CL Item
yes (1)
Item Group
Circulatory Symptoms
C0476270 (UMLS CUI-1)
Item
Thrombophlebitis/Deep Vein Thrombosis
integer
C0040046 (UMLS CUI [1])
C0149871 (UMLS CUI [2])
Code List
Thrombophlebitis/Deep Vein Thrombosis
CL Item
no (0)
CL Item
yes (1)
Item
Pulmonary Embolus
integer
C0034065 (UMLS CUI [1])
Code List
Pulmonary Embolus
CL Item
no (0)
CL Item
yes (1)
Item
Cerebrovascular Accident
integer
C0038454 (UMLS CUI [1])
Code List
Cerebrovascular Accident
CL Item
no (0)
CL Item
yes (1)
Item
Amputation
integer
C0002688 (UMLS CUI [1])
Code List
Amputation
CL Item
no (0)
CL Item
yes (1)
Item
Myocardial Infarction
integer
C0027051 (UMLS CUI [1])
Code List
Myocardial Infarction
CL Item
no (0)
CL Item
yes (1)
Item
Transient Ischemic Attack
integer
C0007787 (UMLS CUI [1])
Code List
Transient Ischemic Attack
CL Item
no (0)
CL Item
yes (1)
Item
Unstable Angina
integer
C0002965 (UMLS CUI [1])
Code List
Unstable Angina
CL Item
no (0)
CL Item
yes (1)
Item
Renal Vein Thrombosis
integer
C0238457 (UMLS CUI [1])
Code List
Renal Vein Thrombosis
CL Item
no (0)
CL Item
yes (1)
Item
Mesenteric Vein Thrombosis
integer
C0267412 (UMLS CUI [1])
Code List
Mesenteric Vein Thrombosis
CL Item
no (0)
CL Item
yes (1)
Item
Portal Vein Thrombosis (Budd-Chiari)
integer
C0155773 (UMLS CUI [1])
Code List
Portal Vein Thrombosis (Budd-Chiari)
CL Item
no (0)
CL Item
yes (1)
Item
Gangrene
integer
C0017086 (UMLS CUI [1])
CL Item
no (0)
CL Item
yes (1)
Item
Acute Peripheral Vascular Occlusion
integer
C0240728 (UMLS CUI [1])
Code List
Acute Peripheral Vascular Occlusion
CL Item
no (0)
CL Item
yes (1)
Item
Sudden Death
integer
C0011071 (UMLS CUI [1])
CL Item
no (0)
CL Item
yes (1)
Item
Patient suffers from other accompanying illnesses?
integer
C0009488 (UMLS CUI [1])
Code List
Patient suffers from other accompanying illnesses?
CL Item
no (0)
CL Item
yes (1)
Item
Only for Woman (under 50): Is the pregnancy test negativ?
integer
C0032976 (UMLS CUI [1])
Code List
Only for Woman (under 50): Is the pregnancy test negativ?
CL Item
no (0)
CL Item
yes (1)
Comments
Item
Comments
text
C0947611 (UMLS CUI [1])
Item Group
Signature principal investigator
C1519316 (UMLS CUI-1)
C1521895 (UMLS CUI-2)
Signature date
Item
Signature date
text
C0807937 (UMLS CUI [1])
Item
Signature investigator
integer
C2346576 (UMLS CUI [1])
Code List
Signature investigator
CL Item
no (0)
CL Item
yes (1)

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