ID
31260
Beschreibung
A Study to Assess the Effects of Naproxcinod and Naproxen on Blood Pressure Measurements in Osteoarthritis Patients With Controlled High Blood Pressure; ODM derived from: https://clinicaltrials.gov/show/NCT00662610
Link
https://clinicaltrials.gov/show/NCT00662610
Stichworte
Versionen (1)
- 04.08.18 04.08.18 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
4. August 2018
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Osteoarthritis NCT00662610
Eligibility Osteoarthritis NCT00662610
- StudyEvent: Eligibility
Beschreibung
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschreibung
Antihypertensive Agents Class Quantity
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0003364
- UMLS CUI [1,2]
- C0456387
- UMLS CUI [1,3]
- C1265611
Beschreibung
Diabetic - poor control
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0421258
Beschreibung
Hepatic impairment | Renal Insufficiency
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0948807
- UMLS CUI [2]
- C1565489
Beschreibung
Substance Use Disorders
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0038586
Beschreibung
Gastric ulcer | Duodenal Ulcer | Gastroduodenal haemorrhage
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0038358
- UMLS CUI [2]
- C0013295
- UMLS CUI [3]
- C1096494
Beschreibung
Congestive heart failure
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0018802
Beschreibung
ECG abnormal
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0522055
Beschreibung
Anticoagulants | Anticoagulants Expected
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0003280
- UMLS CUI [2,1]
- C0003280
- UMLS CUI [2,2]
- C1517001
Beschreibung
Disease Interferes with Study Protocol | Disease At risk Patient safety
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0521102
- UMLS CUI [1,3]
- C2348563
- UMLS CUI [2,1]
- C0012634
- UMLS CUI [2,2]
- C1444641
- UMLS CUI [2,3]
- C1113679
Beschreibung
Study Subject Participation Status | Clinical Trial
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2348568
- UMLS CUI [2]
- C0008976
Ähnliche Modelle
Eligibility Osteoarthritis NCT00662610
- StudyEvent: Eligibility
C0029410 (UMLS CUI [2])
C0409959 (UMLS CUI [3])
C0085580 (UMLS CUI [2,1])
C1522326 (UMLS CUI [2,2])
C0085580 (UMLS CUI [3,1])
C2911690 (UMLS CUI [3,2])
C1265611 (UMLS CUI [1,2])
C0012798 (UMLS CUI [2])
C0003015 (UMLS CUI [3])
C0521942 (UMLS CUI [4])
C0001645 (UMLS CUI [5])
C0205191 (UMLS CUI [1,2])
C0000970 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
C1272691 (UMLS CUI [1,2])
C0456387 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C1565489 (UMLS CUI [2])
C0013295 (UMLS CUI [2])
C1096494 (UMLS CUI [3])
C0003280 (UMLS CUI [2,1])
C1517001 (UMLS CUI [2,2])
C0521102 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
C0012634 (UMLS CUI [2,1])
C1444641 (UMLS CUI [2,2])
C1113679 (UMLS CUI [2,3])
C0008976 (UMLS CUI [2])