ID

29953

Beschrijving

Nifedipine (Adalat CR, BAY A1040) High Dose PK/PD Study; ODM derived from: https://clinicaltrials.gov/show/NCT00768560

Link

https://clinicaltrials.gov/show/NCT00768560

Trefwoorden

Versies (1)
  1. 29-04-18 29-04-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

29 april 2018

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Hypertension NCT00768560

Engels

Eligibility Hypertension NCT00768560

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female
Beschrijving

Gender

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
20 years or older and less than 75 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
outpatient
Beschrijving

Outpatients

Datatype

boolean

Alias
UMLS CUI [1]
C0029921
untreated or treated patients with antihypertensive agents whose blood pressure (bp) in sitting position at entry (visit 1) is as follows.
Beschrijving

Patients untreated | Patients Treated | Antihypertensive Agents | Sitting blood pressure

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0332155
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C1522326
UMLS CUI [3]
C0003364
UMLS CUI [4]
C0580946
untreated patients: systolic blood pressure (sbp) >= 160mmhg or diastolic blood pressure (dbp) >= 100mmhg
Beschrijving

Patients untreated | Systolic Pressure | Diastolic blood pressure

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0332155
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
treated patients: sbp >= 140mmhg or dbp >= 90mmhg (at trough)
Beschrijving

Patients Treated | Systolic Pressure | Diastolic blood pressure

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1522326
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients whose bp during baseline treatment period is: sbp>=200mmhg or dbp>=120mmhg.
Beschrijving

Blood Pressure During Therapeutic procedure | Systolic Pressure | Diastolic blood pressure

Datatype

boolean

Alias
UMLS CUI [1,1]
C0005823
UMLS CUI [1,2]
C0347984
UMLS CUI [1,3]
C0087111
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
patients with secondary hypertension or hypertensive emergency.
Beschrijving

Secondary hypertension | Hypertensive emergency

Datatype

boolean

Alias
UMLS CUI [1]
C0155616
UMLS CUI [2]
C0745136
patients with cardiovascular or cerebrovascular ischemic event (stroke, transient ischemic attack (tia), myocardial infarction or unstable angina), or with history of these within 6 months prior to the study.
Beschrijving

Cardiovascular event | Event cerebrovascular ischemic | Cerebrovascular accident | Transient Ischemic Attack | Myocardial Infarction | Angina, Unstable

Datatype

boolean

Alias
UMLS CUI [1]
C1320716
UMLS CUI [2,1]
C0441471
UMLS CUI [2,2]
C0917798
UMLS CUI [3]
C0038454
UMLS CUI [4]
C0007787
UMLS CUI [5]
C0027051
UMLS CUI [6]
C0002965
patients with intracranial or subarachnoid hemorrhage, or with history of these within 6 months prior to the study.
Beschrijving

Intracranial Hemorrhages | Subarachnoid Hemorrhage

Datatype

boolean

Alias
UMLS CUI [1]
C0151699
UMLS CUI [2]
C0038525
patients with server hematopoietic dysfunction (acute/chronic leukemia, myeloma, malignant lymphoma, myelodysplastic syndrome, aplastic anemia), or with history of these.
Beschrijving

Dysfunction Hematopoietic Severe | Leukemia | Chronic leukemia | Myeloma | Lymphoma | MYELODYSPLASTIC SYNDROME | Aplastic Anemia

Datatype

boolean

Alias
UMLS CUI [1,1]
C3887504
UMLS CUI [1,2]
C0229601
UMLS CUI [1,3]
C0205082
UMLS CUI [2]
C0023418
UMLS CUI [3]
C1279296
UMLS CUI [4]
C0026764
UMLS CUI [5]
C0024299
UMLS CUI [6]
C3463824
UMLS CUI [7]
C0002874
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Similar models

Eligibility Hypertension NCT00768560

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
male and female
boolean
C0079399 (UMLS CUI [1])
Age
Item
20 years or older and less than 75 years
boolean
C0001779 (UMLS CUI [1])
Outpatients
Item
outpatient
boolean
C0029921 (UMLS CUI [1])
Patients untreated | Patients Treated | Antihypertensive Agents | Sitting blood pressure
Item
untreated or treated patients with antihypertensive agents whose blood pressure (bp) in sitting position at entry (visit 1) is as follows.
boolean
C0030705 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0030705 (UMLS CUI [2,1])
C1522326 (UMLS CUI [2,2])
C0003364 (UMLS CUI [3])
C0580946 (UMLS CUI [4])
Patients untreated | Systolic Pressure | Diastolic blood pressure
Item
untreated patients: systolic blood pressure (sbp) >= 160mmhg or diastolic blood pressure (dbp) >= 100mmhg
boolean
C0030705 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Patients Treated | Systolic Pressure | Diastolic blood pressure
Item
treated patients: sbp >= 140mmhg or dbp >= 90mmhg (at trough)
boolean
C0030705 (UMLS CUI [1,1])
C1522326 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Blood Pressure During Therapeutic procedure | Systolic Pressure | Diastolic blood pressure
Item
patients whose bp during baseline treatment period is: sbp>=200mmhg or dbp>=120mmhg.
boolean
C0005823 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Secondary hypertension | Hypertensive emergency
Item
patients with secondary hypertension or hypertensive emergency.
boolean
C0155616 (UMLS CUI [1])
C0745136 (UMLS CUI [2])
Cardiovascular event | Event cerebrovascular ischemic | Cerebrovascular accident | Transient Ischemic Attack | Myocardial Infarction | Angina, Unstable
Item
patients with cardiovascular or cerebrovascular ischemic event (stroke, transient ischemic attack (tia), myocardial infarction or unstable angina), or with history of these within 6 months prior to the study.
boolean
C1320716 (UMLS CUI [1])
C0441471 (UMLS CUI [2,1])
C0917798 (UMLS CUI [2,2])
C0038454 (UMLS CUI [3])
C0007787 (UMLS CUI [4])
C0027051 (UMLS CUI [5])
C0002965 (UMLS CUI [6])
Intracranial Hemorrhages | Subarachnoid Hemorrhage
Item
patients with intracranial or subarachnoid hemorrhage, or with history of these within 6 months prior to the study.
boolean
C0151699 (UMLS CUI [1])
C0038525 (UMLS CUI [2])
Dysfunction Hematopoietic Severe | Leukemia | Chronic leukemia | Myeloma | Lymphoma | MYELODYSPLASTIC SYNDROME | Aplastic Anemia
Item
patients with server hematopoietic dysfunction (acute/chronic leukemia, myeloma, malignant lymphoma, myelodysplastic syndrome, aplastic anemia), or with history of these.
boolean
C3887504 (UMLS CUI [1,1])
C0229601 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
C0023418 (UMLS CUI [2])
C1279296 (UMLS CUI [3])
C0026764 (UMLS CUI [4])
C0024299 (UMLS CUI [5])
C3463824 (UMLS CUI [6])
C0002874 (UMLS CUI [7])
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