Information:
Error:
ID
22256
Description
Analgesic Efficacy and Safety Study of Naproxcinod in Subjects With Osteoarthritis of the Knee; ODM derived from: https://clinicaltrials.gov/show/NCT00542555
Link
https://clinicaltrials.gov/show/NCT00542555
Keywords
Versions (1)
- 5/26/17 5/26/17 -
Uploaded on
May 26, 2017
DOI
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License
Creative Commons BY 4.0
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Eligibility Osteoarthritis NCT00542555
Eligibility Osteoarthritis NCT00542555
- StudyEvent: Eligibility
Similar models
Eligibility Osteoarthritis NCT00542555
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Age | Primary osteoarthritis of knee
Item
men and women (40 or older) with a diagnosis of primary oa of the knee
boolean
C0001779 (UMLS CUI [1])
C2893931 (UMLS CUI [2])
C2893931 (UMLS CUI [2])
Non-Steroidal Anti-Inflammatory Agents chronic | Acetaminophen chronic
Item
must be a current chronic user of nsaids or acetaminophen
boolean
C0003211 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C0000970 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
C0205191 (UMLS CUI [1,2])
C0000970 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
Analgesic therapy To be stopped
Item
must discontinue all analgesic therapy at screening
boolean
C0412784 (UMLS CUI [1,1])
C1272691 (UMLS CUI [1,2])
C1272691 (UMLS CUI [1,2])
Uncontrolled hypertension | Diabetic - poor control
Item
uncontrolled hypertension or diabetes
boolean
C1868885 (UMLS CUI [1])
C0421258 (UMLS CUI [2])
C0421258 (UMLS CUI [2])
Hepatic impairment | Renal Insufficiency
Item
hepatic or renal impairment
boolean
C0948807 (UMLS CUI [1])
C1565489 (UMLS CUI [2])
C1565489 (UMLS CUI [2])
Anticoagulants | Anticoagulants Expected
Item
current or expected use of anticoagulant
boolean
C0003280 (UMLS CUI [1])
C0003280 (UMLS CUI [2,1])
C1517001 (UMLS CUI [2,2])
C0003280 (UMLS CUI [2,1])
C1517001 (UMLS CUI [2,2])
Substance Use Disorders
Item
a history of alcohol or drug abuse
boolean
C0038586 (UMLS CUI [1])
Joint replacement Anticipated
Item
candidates for imminent joint replacement
boolean
C0185317 (UMLS CUI [1,1])
C3840775 (UMLS CUI [1,2])
C3840775 (UMLS CUI [1,2])
Gastric ulcer | Duodenal Ulcer | Gastroduodenal haemorrhage
Item
diagnosis of gastric or duodenal ulceration and/or history of significant gastro-duodenal bleeding, within the last 6 months
boolean
C0038358 (UMLS CUI [1])
C0013295 (UMLS CUI [2])
C1096494 (UMLS CUI [3])
C0013295 (UMLS CUI [2])
C1096494 (UMLS CUI [3])
Disease Interferes with Evaluation
Item
current medical disease that could confound or interfere with the evaluation of efficacy
boolean
C0012634 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0220825 (UMLS CUI [1,3])
C0521102 (UMLS CUI [1,2])
C0220825 (UMLS CUI [1,3])
Study Subject Participation Status
Item
participation within 30 days prior to screening in another investigational study
boolean
C2348568 (UMLS CUI [1])