ID

31296

Beschrijving

Comparative Study of Olive Oil With Piroxicam Gel in Osteoarthritis of the Knee; ODM derived from: https://clinicaltrials.gov/show/NCT00670475

Link

https://clinicaltrials.gov/show/NCT00670475

Trefwoorden

Versies (1)
  1. 09-08-18 09-08-18 -
Houder van rechten

See clinicaltrials.gov

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9 augustus 2018

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Osteoarthritis of the Knee NCT00670475

Engels

Eligibility Osteoarthritis of the Knee NCT00670475

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
men and non-pregnant women, age 40-85 years with primary oa of at least one knee, and a flare of pain after withdrawal of prior therapy with either an oral nsaid or acetaminophen (used at least 3 days per week during the previous month).
Beschrijving

Gender | Pregnancy Absent | Age | Idiopathic osteoarthritis Knee Quantity | Flare Pain | Status post Withdrawal Prior Therapy | NSAID Oral | Acetaminophen Oral

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0032961
UMLS CUI [2,2]
C0332197
UMLS CUI [3]
C0001779
UMLS CUI [4,1]
C0409952
UMLS CUI [4,2]
C0022742
UMLS CUI [4,3]
C1265611
UMLS CUI [5,1]
C1517205
UMLS CUI [5,2]
C0030193
UMLS CUI [6,1]
C0231290
UMLS CUI [6,2]
C2349954
UMLS CUI [6,3]
C1514463
UMLS CUI [7,1]
C0003211
UMLS CUI [7,2]
C1527415
UMLS CUI [8,1]
C0000970
UMLS CUI [8,2]
C1527415
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
secondary arthritis related to systemic inflammatory arthritis (including rheumatoid arthritis, psoriatic arthritis, post-infectious arthritis and metabolic arthritis, traumatic arthritis or surgical joint replacement); corticosteroid use:
Beschrijving

Arthritis Secondary to Arthritis Systemic | Rheumatoid Arthritis | Arthritis, Psoriatic | Arthritis, Reactive | Arthritis, Gouty | Traumatic arthropathy | Joint Replacement | Corticosteroid use

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003864
UMLS CUI [1,2]
C0175668
UMLS CUI [1,3]
C0003864
UMLS CUI [1,4]
C0205373
UMLS CUI [2]
C0003873
UMLS CUI [3]
C0003872
UMLS CUI [4]
C0085435
UMLS CUI [5]
C0003868
UMLS CUI [6]
C0152086
UMLS CUI [7]
C0185317
UMLS CUI [8]
C0239126
oral corticosteroid within the previous 14 days, or
Beschrijving

Adrenal Cortex Hormones Oral

Datatype

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C1527415
intramuscular corticosteroid within 30 days, or
Beschrijving

Adrenal Cortex Hormones Intramuscular

Datatype

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C1556154
intraarticular corticosteroid into the study knee within 90 days,
Beschrijving

Intraarticular injection of corticosteroids Index Knee

Datatype

boolean

Alias
UMLS CUI [1,1]
C2064783
UMLS CUI [1,2]
C2986546
UMLS CUI [1,3]
C0022742
intra-articular corticosteroid into any other joint within 30 days, or
Beschrijving

Intraarticular injection of corticosteroids Joint Other

Datatype

boolean

Alias
UMLS CUI [1,1]
C2064783
UMLS CUI [1,2]
C0022417
UMLS CUI [1,3]
C0205394
topical corticosteroid at the site of application within 14 days;
Beschrijving

Topical corticosteroids Application site

Datatype

boolean

Alias
UMLS CUI [1,1]
C0304604
UMLS CUI [1,2]
C0229986
ongoing use of prohibited medication including nsaid, other oral analgesic, muscle relaxant, or low-dose antidepressant for any chronic pain management; -
Beschrijving

Illicit medication use | Anti-Inflammatory Agents, Non-Steroidal | Analgesics Oral Other | Muscle relaxants | Antidepressive Agents Low dose Chronic pain Management

Datatype

boolean

Alias
UMLS CUI [1]
C0281875
UMLS CUI [2]
C0003211
UMLS CUI [3,1]
C0002771
UMLS CUI [3,2]
C1527415
UMLS CUI [3,3]
C0205394
UMLS CUI [4]
C0358430
UMLS CUI [5,1]
C0003289
UMLS CUI [5,2]
C0445550
UMLS CUI [5,3]
C0150055
UMLS CUI [5,4]
C0376636
ongoing use of glucosamine or chondroitin (unless used continuously for 90 days prior to study entry);
Beschrijving

Glucosamine | Chondroitin

Datatype

boolean

Alias
UMLS CUI [1]
C0017718
UMLS CUI [2]
C0008454
sensitivity to diclofenac, acetylsalicylic acid (asa) or any other nsaid, acetaminophen, dimethyl sulphoxide, propylene glycol, glycerine or ethanol; clinically-active renal, hepatic or peptic ulcer disease;
Beschrijving

Diclofenac allergy | Aspirin allergy | Allergy to nonsteroidal anti-inflammatory agents | Allergy to acetaminophen | Dimethyl sulfoxide allergy | Hypersensitivity Propylene glycol | Hypersensitivity Glycerin | Allergy to ethanol | Kidney Disease | Liver disease | Peptic Ulcer

Datatype

boolean

Alias
UMLS CUI [1]
C0570540
UMLS CUI [2]
C0004058
UMLS CUI [3]
C0746949
UMLS CUI [4]
C0570513
UMLS CUI [5]
C0570718
UMLS CUI [6,1]
C0020517
UMLS CUI [6,2]
C0072225
UMLS CUI [7,1]
C0020517
UMLS CUI [7,2]
C0017861
UMLS CUI [8]
C0740909
UMLS CUI [9]
C0022658
UMLS CUI [10]
C0023895
UMLS CUI [11]
C0030920
history of alcohol or drug abuse;
Beschrijving

Substance Use Disorders

Datatype

boolean

Alias
UMLS CUI [1]
C0038586
lactation;
Beschrijving

Lactation

Datatype

boolean

Alias
UMLS CUI [1]
C0022925
concomitant skin disease at the application site;
Beschrijving

Dermatologic disorder Application site

Datatype

boolean

Alias
UMLS CUI [1,1]
C0037274
UMLS CUI [1,2]
C0229986
current application for disability benefits on the basis of knee osteoarthritis; fibromyalgia; other painful or disabling condition affecting the knee;
Beschrijving

Application Disability Benefits | Osteoarthritis, Knee | Fibromyalgia | Condition Painful Affecting Knee | Disabling disease Affecting Knee

Datatype

boolean

Alias
UMLS CUI [1,1]
C0185125
UMLS CUI [1,2]
C0231170
UMLS CUI [1,3]
C0814225
UMLS CUI [2]
C0409959
UMLS CUI [3]
C0016053
UMLS CUI [4,1]
C0348080
UMLS CUI [4,2]
C0030193
UMLS CUI [4,3]
C0392760
UMLS CUI [4,4]
C0022742
UMLS CUI [5,1]
C0596452
UMLS CUI [5,2]
C0392760
UMLS CUI [5,3]
C0022742
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Similar models

Eligibility Osteoarthritis of the Knee NCT00670475

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Pregnancy Absent | Age | Idiopathic osteoarthritis Knee Quantity | Flare Pain | Status post Withdrawal Prior Therapy | NSAID Oral | Acetaminophen Oral
Item
men and non-pregnant women, age 40-85 years with primary oa of at least one knee, and a flare of pain after withdrawal of prior therapy with either an oral nsaid or acetaminophen (used at least 3 days per week during the previous month).
boolean
C0079399 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0001779 (UMLS CUI [3])
C0409952 (UMLS CUI [4,1])
C0022742 (UMLS CUI [4,2])
C1265611 (UMLS CUI [4,3])
C1517205 (UMLS CUI [5,1])
C0030193 (UMLS CUI [5,2])
C0231290 (UMLS CUI [6,1])
C2349954 (UMLS CUI [6,2])
C1514463 (UMLS CUI [6,3])
C0003211 (UMLS CUI [7,1])
C1527415 (UMLS CUI [7,2])
C0000970 (UMLS CUI [8,1])
C1527415 (UMLS CUI [8,2])
Item Group
C0680251 (UMLS CUI)
Arthritis Secondary to Arthritis Systemic | Rheumatoid Arthritis | Arthritis, Psoriatic | Arthritis, Reactive | Arthritis, Gouty | Traumatic arthropathy | Joint Replacement | Corticosteroid use
Item
secondary arthritis related to systemic inflammatory arthritis (including rheumatoid arthritis, psoriatic arthritis, post-infectious arthritis and metabolic arthritis, traumatic arthritis or surgical joint replacement); corticosteroid use:
boolean
C0003864 (UMLS CUI [1,1])
C0175668 (UMLS CUI [1,2])
C0003864 (UMLS CUI [1,3])
C0205373 (UMLS CUI [1,4])
C0003873 (UMLS CUI [2])
C0003872 (UMLS CUI [3])
C0085435 (UMLS CUI [4])
C0003868 (UMLS CUI [5])
C0152086 (UMLS CUI [6])
C0185317 (UMLS CUI [7])
C0239126 (UMLS CUI [8])
Adrenal Cortex Hormones Oral
Item
oral corticosteroid within the previous 14 days, or
boolean
C0001617 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
Adrenal Cortex Hormones Intramuscular
Item
intramuscular corticosteroid within 30 days, or
boolean
C0001617 (UMLS CUI [1,1])
C1556154 (UMLS CUI [1,2])
Intraarticular injection of corticosteroids Index Knee
Item
intraarticular corticosteroid into the study knee within 90 days,
boolean
C2064783 (UMLS CUI [1,1])
C2986546 (UMLS CUI [1,2])
C0022742 (UMLS CUI [1,3])
Intraarticular injection of corticosteroids Joint Other
Item
intra-articular corticosteroid into any other joint within 30 days, or
boolean
C2064783 (UMLS CUI [1,1])
C0022417 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
Topical corticosteroids Application site
Item
topical corticosteroid at the site of application within 14 days;
boolean
C0304604 (UMLS CUI [1,1])
C0229986 (UMLS CUI [1,2])
Illicit medication use | Anti-Inflammatory Agents, Non-Steroidal | Analgesics Oral Other | Muscle relaxants | Antidepressive Agents Low dose Chronic pain Management
Item
ongoing use of prohibited medication including nsaid, other oral analgesic, muscle relaxant, or low-dose antidepressant for any chronic pain management; -
boolean
C0281875 (UMLS CUI [1])
C0003211 (UMLS CUI [2])
C0002771 (UMLS CUI [3,1])
C1527415 (UMLS CUI [3,2])
C0205394 (UMLS CUI [3,3])
C0358430 (UMLS CUI [4])
C0003289 (UMLS CUI [5,1])
C0445550 (UMLS CUI [5,2])
C0150055 (UMLS CUI [5,3])
C0376636 (UMLS CUI [5,4])
Glucosamine | Chondroitin
Item
ongoing use of glucosamine or chondroitin (unless used continuously for 90 days prior to study entry);
boolean
C0017718 (UMLS CUI [1])
C0008454 (UMLS CUI [2])
Diclofenac allergy | Aspirin allergy | Allergy to nonsteroidal anti-inflammatory agents | Allergy to acetaminophen | Dimethyl sulfoxide allergy | Hypersensitivity Propylene glycol | Hypersensitivity Glycerin | Allergy to ethanol | Kidney Disease | Liver disease | Peptic Ulcer
Item
sensitivity to diclofenac, acetylsalicylic acid (asa) or any other nsaid, acetaminophen, dimethyl sulphoxide, propylene glycol, glycerine or ethanol; clinically-active renal, hepatic or peptic ulcer disease;
boolean
C0570540 (UMLS CUI [1])
C0004058 (UMLS CUI [2])
C0746949 (UMLS CUI [3])
C0570513 (UMLS CUI [4])
C0570718 (UMLS CUI [5])
C0020517 (UMLS CUI [6,1])
C0072225 (UMLS CUI [6,2])
C0020517 (UMLS CUI [7,1])
C0017861 (UMLS CUI [7,2])
C0740909 (UMLS CUI [8])
C0022658 (UMLS CUI [9])
C0023895 (UMLS CUI [10])
C0030920 (UMLS CUI [11])
Substance Use Disorders
Item
history of alcohol or drug abuse;
boolean
C0038586 (UMLS CUI [1])
Lactation
Item
lactation;
boolean
C0022925 (UMLS CUI [1])
Dermatologic disorder Application site
Item
concomitant skin disease at the application site;
boolean
C0037274 (UMLS CUI [1,1])
C0229986 (UMLS CUI [1,2])
Application Disability Benefits | Osteoarthritis, Knee | Fibromyalgia | Condition Painful Affecting Knee | Disabling disease Affecting Knee
Item
current application for disability benefits on the basis of knee osteoarthritis; fibromyalgia; other painful or disabling condition affecting the knee;
boolean
C0185125 (UMLS CUI [1,1])
C0231170 (UMLS CUI [1,2])
C0814225 (UMLS CUI [1,3])
C0409959 (UMLS CUI [2])
C0016053 (UMLS CUI [3])
C0348080 (UMLS CUI [4,1])
C0030193 (UMLS CUI [4,2])
C0392760 (UMLS CUI [4,3])
C0022742 (UMLS CUI [4,4])
C0596452 (UMLS CUI [5,1])
C0392760 (UMLS CUI [5,2])
C0022742 (UMLS CUI [5,3])
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