ID

31282

Description

Efficacy Study of "Go On" in Magnetic Resonance Imaging (MRI) Improvement in Osteoarthritis (OA) Knee; ODM derived from: https://clinicaltrials.gov/show/NCT00750724

Link

https://clinicaltrials.gov/show/NCT00750724

Keywords

Versions (2)
  1. 8/7/18 8/7/18 -
  2. 8/7/18 8/7/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

August 7, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Osteoarthritis NCT00750724

English

Eligibility Osteoarthritis NCT00750724

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects who are capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Description

Informed Consent | Protocol Compliance

Data type

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0525058
ambulatory non pregnant females and males 40-<80 years of age.
Description

Outpatients | Gender | Pregnancy Absent | Age

Data type

boolean

Alias
UMLS CUI [1]
C0029921
UMLS CUI [2]
C0079399
UMLS CUI [3,1]
C0032961
UMLS CUI [3,2]
C0332197
UMLS CUI [4]
C0001779
subjects who withdraw pain medication or nutritional supplements for symptom relief for oa hand for a total of at least 30 days before screening visit 0.
Description

Analgesics Withdrawn | Dietary Supplements Withdrawn | Symptom Relief Osteoarthritis of the hand

Data type

boolean

Alias
UMLS CUI [1,1]
C0002771
UMLS CUI [1,2]
C0424092
UMLS CUI [2,1]
C0242295
UMLS CUI [2,2]
C0424092
UMLS CUI [3,1]
C1457887
UMLS CUI [3,2]
C0564405
UMLS CUI [3,3]
C0263746
pain at or below 40 mm on a 100 mm vas in the index knee joints.
Description

Index Knee joint pain Visual Analog Pain Scale

Data type

boolean

Alias
UMLS CUI [1,1]
C2986546
UMLS CUI [1,2]
C0231749
UMLS CUI [1,3]
C0042815
a documented diagnosis of oa of the knee joint, or meeting american college of rheumatology (acr) clinical criteria for classification of idiopathic (primary) oa for at least 6 months prior to screening.
Description

Osteoarthritis Knee joint | Idiopathic osteoarthritis Duration

Data type

boolean

Alias
UMLS CUI [1,1]
C0029408
UMLS CUI [1,2]
C0022745
UMLS CUI [2,1]
C0409952
UMLS CUI [2,2]
C0449238
subject has been documented radiographic evidence of oa of the knees from the screening visit radiograph of grade 2 or 3 according to kellgren and lawrence radiographic grading.
Description

Knee Osteoarthritis Kellgren-Lawrence score Radiography

Data type

boolean

Alias
UMLS CUI [1,1]
C0409959
UMLS CUI [1,2]
C3177117
UMLS CUI [1,3]
C0034571
subject has no any contraindication for mri
Description

Medical contraindication Absent MRI

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C0024485
subject is able to understand and complete pain/function, global arthritis evaluation, and health outcome assessment.
Description

Comprehension Pain level | Comprehension Level of function | Comprehension Evaluation Arthritis | Comprehension Outcome Assessment (Health Care) | Completion Pain level | Completion Level of function | Completion Evaluation Arthritis | Completion Outcome Assessment (Health Care)

Data type

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C0518087
UMLS CUI [2,1]
C0162340
UMLS CUI [2,2]
C0935587
UMLS CUI [3,1]
C0162340
UMLS CUI [3,2]
C1261322
UMLS CUI [3,3]
C0003864
UMLS CUI [4,1]
C0162340
UMLS CUI [4,2]
C0085565
UMLS CUI [5,1]
C0205197
UMLS CUI [5,2]
C0518087
UMLS CUI [6,1]
C0205197
UMLS CUI [6,2]
C0935587
UMLS CUI [7,1]
C0205197
UMLS CUI [7,2]
C1261322
UMLS CUI [7,3]
C0003864
UMLS CUI [8,1]
C0205197
UMLS CUI [8,2]
C0085565
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects with history of hypersensitivity to hyaluronate.
Description

Hypersensitivity Hyaluronate

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0178695
subjects with skin lesion at the knee joint.
Description

Skin lesion Knee joint

Data type

boolean

Alias
UMLS CUI [1,1]
C0037284
UMLS CUI [1,2]
C0022745
a history of knee surgery within 6 months prior to screening v0.
Description

Operative procedure on knee

Data type

boolean

Alias
UMLS CUI [1]
C0187769
significant prior injury to the knee joint within 12 months prior to screening v0.
Description

Injury Knee joint

Data type

boolean

Alias
UMLS CUI [1,1]
C3263722
UMLS CUI [1,2]
C0022745
disease of the spine or other lower extremity joints of sufficient degree to affect the knee joint.
Description

Spinal Disease Affecting Knee joint | Disease Joint of lower extremity Affecting Knee joint

Data type

boolean

Alias
UMLS CUI [1,1]
C0037933
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0022745
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C0584731
UMLS CUI [2,3]
C0392760
UMLS CUI [2,4]
C0022745
treatment with other drugs potentially affecting bone or cartilage metabolism as described below:
Description

Pharmaceutical Preparations Affecting Bone metabolism | Pharmaceutical Preparations Affecting Cartilage metabolism

Data type

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0596204
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C0596276
chronic systematic corticosteroids
Description

Adrenal Cortex Hormones systematic chronic

Data type

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C0220922
UMLS CUI [1,3]
C0205191
diacerin or glucosamine treatment within the last 12 months.
Description

Diacetylrhein | Glucosamine

Data type

boolean

Alias
UMLS CUI [1]
C0057678
UMLS CUI [2]
C0017718
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Similar models

Eligibility Osteoarthritis NCT00750724

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent | Protocol Compliance
Item
subjects who are capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
Outpatients | Gender | Pregnancy Absent | Age
Item
ambulatory non pregnant females and males 40-<80 years of age.
boolean
C0029921 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
C0032961 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0001779 (UMLS CUI [4])
Analgesics Withdrawn | Dietary Supplements Withdrawn | Symptom Relief Osteoarthritis of the hand
Item
subjects who withdraw pain medication or nutritional supplements for symptom relief for oa hand for a total of at least 30 days before screening visit 0.
boolean
C0002771 (UMLS CUI [1,1])
C0424092 (UMLS CUI [1,2])
C0242295 (UMLS CUI [2,1])
C0424092 (UMLS CUI [2,2])
C1457887 (UMLS CUI [3,1])
C0564405 (UMLS CUI [3,2])
C0263746 (UMLS CUI [3,3])
Index Knee joint pain Visual Analog Pain Scale
Item
pain at or below 40 mm on a 100 mm vas in the index knee joints.
boolean
C2986546 (UMLS CUI [1,1])
C0231749 (UMLS CUI [1,2])
C0042815 (UMLS CUI [1,3])
Osteoarthritis Knee joint | Idiopathic osteoarthritis Duration
Item
a documented diagnosis of oa of the knee joint, or meeting american college of rheumatology (acr) clinical criteria for classification of idiopathic (primary) oa for at least 6 months prior to screening.
boolean
C0029408 (UMLS CUI [1,1])
C0022745 (UMLS CUI [1,2])
C0409952 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
Knee Osteoarthritis Kellgren-Lawrence score Radiography
Item
subject has been documented radiographic evidence of oa of the knees from the screening visit radiograph of grade 2 or 3 according to kellgren and lawrence radiographic grading.
boolean
C0409959 (UMLS CUI [1,1])
C3177117 (UMLS CUI [1,2])
C0034571 (UMLS CUI [1,3])
Medical contraindication Absent MRI
Item
subject has no any contraindication for mri
boolean
C1301624 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,3])
Comprehension Pain level | Comprehension Level of function | Comprehension Evaluation Arthritis | Comprehension Outcome Assessment (Health Care) | Completion Pain level | Completion Level of function | Completion Evaluation Arthritis | Completion Outcome Assessment (Health Care)
Item
subject is able to understand and complete pain/function, global arthritis evaluation, and health outcome assessment.
boolean
C0162340 (UMLS CUI [1,1])
C0518087 (UMLS CUI [1,2])
C0162340 (UMLS CUI [2,1])
C0935587 (UMLS CUI [2,2])
C0162340 (UMLS CUI [3,1])
C1261322 (UMLS CUI [3,2])
C0003864 (UMLS CUI [3,3])
C0162340 (UMLS CUI [4,1])
C0085565 (UMLS CUI [4,2])
C0205197 (UMLS CUI [5,1])
C0518087 (UMLS CUI [5,2])
C0205197 (UMLS CUI [6,1])
C0935587 (UMLS CUI [6,2])
C0205197 (UMLS CUI [7,1])
C1261322 (UMLS CUI [7,2])
C0003864 (UMLS CUI [7,3])
C0205197 (UMLS CUI [8,1])
C0085565 (UMLS CUI [8,2])
Item Group
C0680251 (UMLS CUI)
Hypersensitivity Hyaluronate
Item
subjects with history of hypersensitivity to hyaluronate.
boolean
C0020517 (UMLS CUI [1,1])
C0178695 (UMLS CUI [1,2])
Skin lesion Knee joint
Item
subjects with skin lesion at the knee joint.
boolean
C0037284 (UMLS CUI [1,1])
C0022745 (UMLS CUI [1,2])
Operative procedure on knee
Item
a history of knee surgery within 6 months prior to screening v0.
boolean
C0187769 (UMLS CUI [1])
Injury Knee joint
Item
significant prior injury to the knee joint within 12 months prior to screening v0.
boolean
C3263722 (UMLS CUI [1,1])
C0022745 (UMLS CUI [1,2])
Spinal Disease Affecting Knee joint | Disease Joint of lower extremity Affecting Knee joint
Item
disease of the spine or other lower extremity joints of sufficient degree to affect the knee joint.
boolean
C0037933 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0022745 (UMLS CUI [1,3])
C0012634 (UMLS CUI [2,1])
C0584731 (UMLS CUI [2,2])
C0392760 (UMLS CUI [2,3])
C0022745 (UMLS CUI [2,4])
Pharmaceutical Preparations Affecting Bone metabolism | Pharmaceutical Preparations Affecting Cartilage metabolism
Item
treatment with other drugs potentially affecting bone or cartilage metabolism as described below:
boolean
C0013227 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0596204 (UMLS CUI [1,3])
C0013227 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0596276 (UMLS CUI [2,3])
Adrenal Cortex Hormones systematic chronic
Item
chronic systematic corticosteroids
boolean
C0001617 (UMLS CUI [1,1])
C0220922 (UMLS CUI [1,2])
C0205191 (UMLS CUI [1,3])
Diacetylrhein | Glucosamine
Item
diacerin or glucosamine treatment within the last 12 months.
boolean
C0057678 (UMLS CUI [1])
C0017718 (UMLS CUI [2])
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