Eligibility Osteoarthritis NCT00542555

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
men and women (40 or older) with a diagnosis of primary oa of the knee
Beskrivning

Age | Primary osteoarthritis of knee

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C2893931
must be a current chronic user of nsaids or acetaminophen
Beskrivning

Non-Steroidal Anti-Inflammatory Agents chronic | Acetaminophen chronic

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0003211
UMLS CUI [1,2]
C0205191
UMLS CUI [2,1]
C0000970
UMLS CUI [2,2]
C0205191
must discontinue all analgesic therapy at screening
Beskrivning

Analgesic therapy To be stopped

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0412784
UMLS CUI [1,2]
C1272691
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
uncontrolled hypertension or diabetes
Beskrivning

Uncontrolled hypertension | Diabetic - poor control

Datatyp

boolean

Alias
UMLS CUI [1]
C1868885
UMLS CUI [2]
C0421258
hepatic or renal impairment
Beskrivning

Hepatic impairment | Renal Insufficiency

Datatyp

boolean

Alias
UMLS CUI [1]
C0948807
UMLS CUI [2]
C1565489
current or expected use of anticoagulant
Beskrivning

Anticoagulants | Anticoagulants Expected

Datatyp

boolean

Alias
UMLS CUI [1]
C0003280
UMLS CUI [2,1]
C0003280
UMLS CUI [2,2]
C1517001
a history of alcohol or drug abuse
Beskrivning

Substance Use Disorders

Datatyp

boolean

Alias
UMLS CUI [1]
C0038586
candidates for imminent joint replacement
Beskrivning

Joint replacement Anticipated

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0185317
UMLS CUI [1,2]
C3840775
diagnosis of gastric or duodenal ulceration and/or history of significant gastro-duodenal bleeding, within the last 6 months
Beskrivning

Gastric ulcer | Duodenal Ulcer | Gastroduodenal haemorrhage

Datatyp

boolean

Alias
UMLS CUI [1]
C0038358
UMLS CUI [2]
C0013295
UMLS CUI [3]
C1096494
current medical disease that could confound or interfere with the evaluation of efficacy
Beskrivning

Disease Interferes with Evaluation

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0220825
participation within 30 days prior to screening in another investigational study
Beskrivning

Study Subject Participation Status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Osteoarthritis NCT00542555

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
Analgesic therapy To be stopped
Item
must discontinue all analgesic therapy at screening
boolean
C0412784 (UMLS CUI [1,1])
C1272691 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Uncontrolled hypertension | Diabetic - poor control
Item
uncontrolled hypertension or diabetes
boolean
C1868885 (UMLS CUI [1])
C0421258 (UMLS CUI [2])
Hepatic impairment | Renal Insufficiency
Item
hepatic or renal impairment
boolean
C0948807 (UMLS CUI [1])
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])
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])
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])
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])
Study Subject Participation Status
Item
participation within 30 days prior to screening in another investigational study
boolean
C2348568 (UMLS CUI [1])