ID

31254

Description

Efficacy of ThermoProfen in Patients With Mild to Moderate Pain Associated With Osteoarthritis of the Knee; ODM derived from: https://clinicaltrials.gov/show/NCT00488267

Lien

https://clinicaltrials.gov/show/NCT00488267

Mots-clés

Versions (1)
  1. 03/08/2018 03/08/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

3 août 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Osteoarthritis NCT00488267

Anglais

Eligibility Osteoarthritis NCT00488267

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient is 18 through 75 years of age
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
patient has radiographic evidence of osteoarthritis of the target knee obtained within the past year.
Description

Osteoarthritis Target Knee Radiography

Type de données

boolean

Alias
UMLS CUI [1,1]
C0409959
UMLS CUI [1,2]
C1521840
UMLS CUI [1,3]
C0034571
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient has a known allergy to nonsteroidal anti-inflammatory drugs (nsaids, including aspirin).
Description

Allergy to nonsteroidal anti-inflammatory agents | Aspirin allergy

Type de données

boolean

Alias
UMLS CUI [1]
C0746949
UMLS CUI [2]
C0004058
patient has asthma that has been induced or made worse by the use of aspirin or nsaids.
Description

Asthma, Aspirin-Induced | Asthma NSAIDs Induced | Asthma Worsened Due to Aspirin | Asthma Worsened Due to NSAIDs

Type de données

boolean

Alias
UMLS CUI [1]
C1319853
UMLS CUI [2,1]
C0004096
UMLS CUI [2,2]
C0003211
UMLS CUI [2,3]
C0205263
UMLS CUI [3,1]
C0004096
UMLS CUI [3,2]
C1457868
UMLS CUI [3,3]
C0678226
UMLS CUI [3,4]
C0004057
UMLS CUI [4,1]
C0004096
UMLS CUI [4,2]
C1457868
UMLS CUI [4,3]
C0678226
UMLS CUI [4,4]
C0003211
patient has a relevant history of serious gastrointestinal disease.
Description

Gastrointestinal Disease Serious

Type de données

boolean

Alias
UMLS CUI [1,1]
C0017178
UMLS CUI [1,2]
C0205404
patient, if female, is pregnant or breastfeeding or is of childbearing potential and not practicing adequate birth control.
Description

Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Absent

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C3831118
UMLS CUI [3,2]
C0700589
UMLS CUI [3,3]
C0332197
patient is taking warfarin, heparin, or low molecular weight heparin.
Description

Warfarin | Heparin | Heparin, Low-Molecular-Weight

Type de données

boolean

Alias
UMLS CUI [1]
C0043031
UMLS CUI [2]
C0019134
UMLS CUI [3]
C0019139
patient has received oral, intramuscular, intravenous, intra-articular, or soft-tissue administration of steroids within 1 month of study enrollment (or within 2 months, if in the target joint).
Description

Steroids Oral | Steroids Intramuscular | Intravenous steroids | Steroids Intraarticular | Steroids Soft Tissue Administration

Type de données

boolean

Alias
UMLS CUI [1,1]
C0038317
UMLS CUI [1,2]
C1527415
UMLS CUI [2,1]
C0038317
UMLS CUI [2,2]
C1556154
UMLS CUI [3]
C0563322
UMLS CUI [4,1]
C0038317
UMLS CUI [4,2]
C1522204
UMLS CUI [5,1]
C0038317
UMLS CUI [5,2]
C1522192
patient has received intra-articular visco-supplementation (in target joint) within 6 months of study enrollment.
Description

Viscosupplementation Target Joint

Type de données

boolean

Alias
UMLS CUI [1,1]
C2350507
UMLS CUI [1,2]
C1521840
UMLS CUI [1,3]
C0022417
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Similar models

Eligibility Osteoarthritis NCT00488267

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
patient is 18 through 75 years of age
boolean
C0001779 (UMLS CUI [1])
Osteoarthritis Target Knee Radiography
Item
patient has radiographic evidence of osteoarthritis of the target knee obtained within the past year.
boolean
C0409959 (UMLS CUI [1,1])
C1521840 (UMLS CUI [1,2])
C0034571 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Allergy to nonsteroidal anti-inflammatory agents | Aspirin allergy
Item
patient has a known allergy to nonsteroidal anti-inflammatory drugs (nsaids, including aspirin).
boolean
C0746949 (UMLS CUI [1])
C0004058 (UMLS CUI [2])
Asthma, Aspirin-Induced | Asthma NSAIDs Induced | Asthma Worsened Due to Aspirin | Asthma Worsened Due to NSAIDs
Item
patient has asthma that has been induced or made worse by the use of aspirin or nsaids.
boolean
C1319853 (UMLS CUI [1])
C0004096 (UMLS CUI [2,1])
C0003211 (UMLS CUI [2,2])
C0205263 (UMLS CUI [2,3])
C0004096 (UMLS CUI [3,1])
C1457868 (UMLS CUI [3,2])
C0678226 (UMLS CUI [3,3])
C0004057 (UMLS CUI [3,4])
C0004096 (UMLS CUI [4,1])
C1457868 (UMLS CUI [4,2])
C0678226 (UMLS CUI [4,3])
C0003211 (UMLS CUI [4,4])
Gastrointestinal Disease Serious
Item
patient has a relevant history of serious gastrointestinal disease.
boolean
C0017178 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Absent
Item
patient, if female, is pregnant or breastfeeding or is of childbearing potential and not practicing adequate birth control.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
Warfarin | Heparin | Heparin, Low-Molecular-Weight
Item
patient is taking warfarin, heparin, or low molecular weight heparin.
boolean
C0043031 (UMLS CUI [1])
C0019134 (UMLS CUI [2])
C0019139 (UMLS CUI [3])
Steroids Oral | Steroids Intramuscular | Intravenous steroids | Steroids Intraarticular | Steroids Soft Tissue Administration
Item
patient has received oral, intramuscular, intravenous, intra-articular, or soft-tissue administration of steroids within 1 month of study enrollment (or within 2 months, if in the target joint).
boolean
C0038317 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C0038317 (UMLS CUI [2,1])
C1556154 (UMLS CUI [2,2])
C0563322 (UMLS CUI [3])
C0038317 (UMLS CUI [4,1])
C1522204 (UMLS CUI [4,2])
C0038317 (UMLS CUI [5,1])
C1522192 (UMLS CUI [5,2])
Viscosupplementation Target Joint
Item
patient has received intra-articular visco-supplementation (in target joint) within 6 months of study enrollment.
boolean
C2350507 (UMLS CUI [1,1])
C1521840 (UMLS CUI [1,2])
C0022417 (UMLS CUI [1,3])
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