ID

31254

Descripción

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

Link

https://clinicaltrials.gov/show/NCT00488267

Palabras clave

  1. 3/8/18 3/8/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

3 de agosto de 2018

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Osteoarthritis NCT00488267

Eligibility Osteoarthritis NCT00488267

Inclusion Criteria
Descripción

Inclusion Criteria

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

Age

Tipo de datos

boolean

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

Osteoarthritis Target Knee Radiography

Tipo de datos

boolean

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

Exclusion Criteria

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

Allergy to nonsteroidal anti-inflammatory agents | Aspirin allergy

Tipo de datos

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.
Descripción

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

Tipo de datos

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.
Descripción

Gastrointestinal Disease Serious

Tipo de datos

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.
Descripción

Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Absent

Tipo de datos

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.
Descripción

Warfarin | Heparin | Heparin, Low-Molecular-Weight

Tipo de datos

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).
Descripción

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

Tipo de datos

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.
Descripción

Viscosupplementation Target Joint

Tipo de datos

boolean

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

Similar models

Eligibility Osteoarthritis NCT00488267

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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