Informationen:
Fehler:
ID
29904
Beschreibung
Pharmacokinetic Drug Interaction Study Following Co-administration of Valsartan, Hydrochlorothiazide and Amlodipine in Patients With Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00548067
Link
https://clinicaltrials.gov/show/NCT00548067
Stichworte
Versionen (1)
- 26.04.18 26.04.18 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
26. April 2018
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Hypertension NCT00548067
Eligibility Hypertension NCT00548067
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Hypertension NCT00548067
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Hypertensive disease
Item
patients diagnosed as hypertensive
boolean
C0020538 (UMLS CUI [1])
Hypertensive disease untreated | Systolic Pressure Consistent | Diastolic blood pressure Consistent
Item
untreated confirmed hypertensive patients (consistent sbp >140 mm hg or dbp >90 mm hg)
boolean
C0020538 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0428883 (UMLS CUI [3,1])
C0332290 (UMLS CUI [3,2])
C0332155 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0428883 (UMLS CUI [3,1])
C0332290 (UMLS CUI [3,2])
Hypertensive disease Uncontrolled | Systolic Pressure Consistent | Diastolic blood pressure Consistent | Pharmacotherapy Quantity
Item
uncontrolled hypertensive patients (consistent sbp >140 mm hg or dbp >90 mm hg) on one drug therapy.
boolean
C0020538 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0428883 (UMLS CUI [3,1])
C0332290 (UMLS CUI [3,2])
C0013216 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
C0205318 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0428883 (UMLS CUI [3,1])
C0332290 (UMLS CUI [3,2])
C0013216 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
Hypertensive disease Uncontrolled | Systolic Pressure Consistent | Diastolic blood pressure Consistent | Pharmacotherapy Quantity
Item
uncontrolled hypertensive patients (consistent sbp >140 mm hg or dbp >90 mm hg) on two drug therapy.
boolean
C0020538 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0428883 (UMLS CUI [3,1])
C0332290 (UMLS CUI [3,2])
C0013216 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
C0205318 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0428883 (UMLS CUI [3,1])
C0332290 (UMLS CUI [3,2])
C0013216 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
Antihypertensive Agents | Change of medication Unable
Item
inability to switch from all prior antihypertensive medications safely as required by the protocol.
boolean
C0003364 (UMLS CUI [1])
C0580105 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
C0580105 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Patient need for Pharmaceutical Preparations | Exception Investigational New Drugs
Item
need for drugs other than study drugs at the time of baseline.
boolean
C0686904 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
C0013227 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
Systolic Pressure | Diastolic blood pressure
Item
patients with sbp ≥ 180 mmhg and/or dbp ≥ 110 mmhg at screening.
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
C0428883 (UMLS CUI [2])
Antihypertensive Agents Quantity
Item
patients on four or more antihypertensive drugs at screening.
boolean
C0003364 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant or nursing (lactating) women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Diabetes Mellitus
Item
patients with diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Heart Diseases | Disease Other Any
Item
patients with heart diseases and any other disease
boolean
C0018799 (UMLS CUI [1])
C0012634 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C1552551 (UMLS CUI [2,3])
C0012634 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C1552551 (UMLS CUI [2,3])
Eligibility Criteria Study Protocol
Item
other protocol-defined inclusion/exclusion criteria may apply
boolean
C1516637 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,2])