Informatie:
Fout:
ID
23207
Beschrijving
Safety and Efficacy of Aliskiren 300 mg, 150 mg and 75 mg in Patients With Essential Hypertension Compared to Ramipril 5 mg; ODM derived from: https://clinicaltrials.gov/show/NCT00529451
Link
https://clinicaltrials.gov/show/NCT00529451
Trefwoorden
Versies (1)
- 28-06-17 28-06-17 -
Geüploaded op
28 juni 2017
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Hypertension NCT00529451
Eligibility Hypertension NCT00529451
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT00529451
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
ID.1
Item
patients must have msdbp ≥ 90 mmhg and < 110 mmhg at the visit immediately prior to visit 3
boolean
C0005823 (UMLS CUI [1])
ID.2
Item
patients must have msdbp >or= 95 mmhg and < 110 mmhg at visit 3
boolean
C0005823 (UMLS CUI [1])
ID.3
Item
patients must have an absolute difference of < or =10 mmhg in their mean sitting diastolic blood pressure (msdbp) from visit 2 to visit 3
boolean
C0005823 (UMLS CUI [1,1])
C1705241 (UMLS CUI [1,2])
C1705241 (UMLS CUI [1,2])
ID.4
Item
severe hypertension (grade 3 who classification; msdbp >or= 110 mmhg and/or mssbp >or = 180 mmhg).
boolean
C4013784 (UMLS CUI [1])
ID.5
Item
history or evidence of a secondary form of hypertension.
boolean
C0155616 (UMLS CUI [1])
ID.6
Item
history of transient ischemic cerebral attack within 12 months of visit 1.
boolean
C0007787 (UMLS CUI [1])
ID.7
Item
current angina pectoris requiring pharmacological therapy (other than those patients on a stable dose of oral or topical nitrates)
boolean
C0002962 (UMLS CUI [1])
ID.8
Item
type 1 or type 2 diabetes mellitus with glycosylated hemoglobin (hba1c) > 8% at visit 1.
boolean
C0011849 (UMLS CUI [1])
ID.9
Item
known or suspected contraindications to the study medications, including history of allergy to ramipril or other ace inhibitors.
boolean
C0683526 (UMLS CUI [1,1])
C0571943 (UMLS CUI [1,2])
C0571939 (UMLS CUI [1,3])
C0571943 (UMLS CUI [1,2])
C0571939 (UMLS CUI [1,3])
ID.10
Item
other protocol-defined inclusion/exclusion criteria may apply.
boolean
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
C0680251 (UMLS CUI [1,2])