ID

42731

Descripción

Efficacy Study on Symptomatic Control of Patient With Knee Osteoarthritis Between 0.0125% of Capsaicin to Placebo; ODM derived from: https://clinicaltrials.gov/show/NCT00471055

Link

https://clinicaltrials.gov/show/NCT00471055

Palabras clave

  1. 19/8/17 19/8/17 -
  2. 17/9/21 17/9/21 -
Subido en

17 de septiembre de 2021

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Osteoarthritis, Knee Joint NCT00471055

Eligibility Osteoarthritis, Knee Joint NCT00471055

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects eligible for enrollment in the study must meet all of the following criteria:
Descripción

Criteria Fulfill

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
1. subjects who are capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Descripción

Informed Consent | Protocol Compliance

Tipo de datos

boolean

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

Ambulatory | Pregnancy Absent | Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0439841
UMLS CUI [2,1]
C0032961
UMLS CUI [2,2]
C0332197
UMLS CUI [3]
C0001779
3. subjects who withdraw pain medication or nutritional supplements for symptom relief for knee oa for a total of at least 15 days before screening visit 0.
Descripción

Analgesics Withdrawn | Dietary Supplements Withdrawn | Knee Osteoarthritis Symptoms relief

Tipo de datos

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]
C0409959
UMLS CUI [3,2]
C1457887
UMLS CUI [3,3]
C0564405
4. pain at or below 80 mm on a 100 mm vas in the index knee.
Descripción

Knee pain Visual Analog Pain Scale

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0231749
UMLS CUI [1,2]
C0042815
5. a documented diagnosis of oa of the knee, or meeting american college of rheumatology (acr) clinical criteria for classification of idiopathic (primary) oa for at least 6 months prior to screening. if oa is presented in both knees the investigator will identify which knee will be x-rayed for study entry, with preference for the knee with more severe pain (<80mm vas).
Descripción

Osteoarthritis, Knee | Idiopathic osteoarthritis Disease length | Radiography of knee

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0409959
UMLS CUI [2,1]
C0409952
UMLS CUI [2,2]
C0872146
UMLS CUI [3]
C0845957
6. has documented radiographic evidence of oa of the knee from the screening visit radiograph of grade 2 or 3 according to kellgren and lawrence radiographic grading.
Descripción

Knee Osteoarthritis Kellgren-Lawrence score

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0409959
UMLS CUI [1,2]
C3177117
7. subjects with baseline minimum joint space width in the medial compartment of the index knee of > 1.5 mm at baseline, measured from radiographs using the mtp view.
Descripción

Joint space Width Minimum Medial compartment of knee | Radiography Knee Involved Metatarsophalangeal joint View

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0224497
UMLS CUI [1,2]
C0487742
UMLS CUI [1,3]
C1524031
UMLS CUI [1,4]
C0447799
UMLS CUI [2,1]
C0034571
UMLS CUI [2,2]
C0022742
UMLS CUI [2,3]
C1314939
UMLS CUI [2,4]
C0025589
UMLS CUI [2,5]
C0449911
8. subjects with baseline minimum joint space width in the lateral compartment of the index knee of > 2.5 mm at baseline, measured from radiographs using the mtp view.
Descripción

Joint space Width Minimum Lateral compartment of knee | Radiography Knee Involved Metatarsophalangeal joint View

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0224497
UMLS CUI [1,2]
C0487742
UMLS CUI [1,3]
C1524031
UMLS CUI [1,4]
C0447800
UMLS CUI [2,1]
C0034571
UMLS CUI [2,2]
C0022742
UMLS CUI [2,3]
C1314939
UMLS CUI [2,4]
C0025589
UMLS CUI [2,5]
C0449911
9. subject is able to understand and complete pain/function, global arthritis evaluation, and health outcome assessment.
Descripción

Comprehension Pain | Arthritis Evaluation Global | Therapy Outcome Assessment

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C0030193
UMLS CUI [2,1]
C0003864
UMLS CUI [2,2]
C1261322
UMLS CUI [2,3]
C2348867
UMLS CUI [3,1]
C1518681
UMLS CUI [3,2]
C1516048
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects with any of the following criteria must not be enrolled in the study:
Descripción

Criteria Fulfill

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
1. subjects with history of hypersensitivity to capsaicin.
Descripción

Hypersensitivity Capsaicin

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0006931
2. subjects with skin lesion at the index knee.
Descripción

Skin lesion Knee Involved

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0037284
UMLS CUI [1,2]
C0022742
UMLS CUI [1,3]
C1314939
3. a history of lower extremity surgery within 6 months prior to screening v0.
Descripción

Surgical procedure on lower extremity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0187763
4. significant prior injury to the index knee within 12 months prior to screening v0.
Descripción

Injury Knee Involved

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3263723
UMLS CUI [1,2]
C0022742
UMLS CUI [1,3]
C1314939
5. disease of the spine or other lower extremity joints of sufficient degree to affect the index knee.
Descripción

Spinal Disease Affecting Knee Involved | Disease Lower extremity joint Affecting Knee Involved

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0037933
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0022742
UMLS CUI [1,4]
C1314939
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C0584731
UMLS CUI [2,3]
C0392760
UMLS CUI [2,4]
C0022742
UMLS CUI [2,5]
C1314939
6. treatment with other drugs potentially affecting bone or cartilage metabolism as described below:
Descripción

Pharmaceutical Preparations Affecting Bone metabolism | Pharmaceutical Preparations Affecting Cartilage metabolism

Tipo de datos

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
Descripción

CORTICOSTEROIDS FOR SYSTEMIC USE chronic

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3653708
UMLS CUI [1,2]
C0205191
hyaluronan injection into the index knee with in the previous 6 months.
Descripción

Hyaluronan Injection Knee Involved

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020196
UMLS CUI [1,2]
C1828121
UMLS CUI [1,3]
C0022742
UMLS CUI [1,4]
C1314939
diacerin treatment within the last 12 months.
Descripción

diacetylrhein

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0057678

Similar models

Eligibility Osteoarthritis, Knee Joint NCT00471055

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Criteria Fulfill
Item
subjects eligible for enrollment in the study must meet all of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Informed Consent | Protocol Compliance
Item
1. 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])
Ambulatory | Pregnancy Absent | Age
Item
2. ambulatory nom pregnant females and males 40-<80 years of age.
boolean
C0439841 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0001779 (UMLS CUI [3])
Analgesics Withdrawn | Dietary Supplements Withdrawn | Knee Osteoarthritis Symptoms relief
Item
3. subjects who withdraw pain medication or nutritional supplements for symptom relief for knee oa for a total of at least 15 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])
C0409959 (UMLS CUI [3,1])
C1457887 (UMLS CUI [3,2])
C0564405 (UMLS CUI [3,3])
Knee pain Visual Analog Pain Scale
Item
4. pain at or below 80 mm on a 100 mm vas in the index knee.
boolean
C0231749 (UMLS CUI [1,1])
C0042815 (UMLS CUI [1,2])
Osteoarthritis, Knee | Idiopathic osteoarthritis Disease length | Radiography of knee
Item
5. a documented diagnosis of oa of the knee, or meeting american college of rheumatology (acr) clinical criteria for classification of idiopathic (primary) oa for at least 6 months prior to screening. if oa is presented in both knees the investigator will identify which knee will be x-rayed for study entry, with preference for the knee with more severe pain (<80mm vas).
boolean
C0409959 (UMLS CUI [1])
C0409952 (UMLS CUI [2,1])
C0872146 (UMLS CUI [2,2])
C0845957 (UMLS CUI [3])
Knee Osteoarthritis Kellgren-Lawrence score
Item
6. has documented radiographic evidence of oa of the knee 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])
Joint space Width Minimum Medial compartment of knee | Radiography Knee Involved Metatarsophalangeal joint View
Item
7. subjects with baseline minimum joint space width in the medial compartment of the index knee of > 1.5 mm at baseline, measured from radiographs using the mtp view.
boolean
C0224497 (UMLS CUI [1,1])
C0487742 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,3])
C0447799 (UMLS CUI [1,4])
C0034571 (UMLS CUI [2,1])
C0022742 (UMLS CUI [2,2])
C1314939 (UMLS CUI [2,3])
C0025589 (UMLS CUI [2,4])
C0449911 (UMLS CUI [2,5])
Joint space Width Minimum Lateral compartment of knee | Radiography Knee Involved Metatarsophalangeal joint View
Item
8. subjects with baseline minimum joint space width in the lateral compartment of the index knee of > 2.5 mm at baseline, measured from radiographs using the mtp view.
boolean
C0224497 (UMLS CUI [1,1])
C0487742 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,3])
C0447800 (UMLS CUI [1,4])
C0034571 (UMLS CUI [2,1])
C0022742 (UMLS CUI [2,2])
C1314939 (UMLS CUI [2,3])
C0025589 (UMLS CUI [2,4])
C0449911 (UMLS CUI [2,5])
Comprehension Pain | Arthritis Evaluation Global | Therapy Outcome Assessment
Item
9. subject is able to understand and complete pain/function, global arthritis evaluation, and health outcome assessment.
boolean
C0162340 (UMLS CUI [1,1])
C0030193 (UMLS CUI [1,2])
C0003864 (UMLS CUI [2,1])
C1261322 (UMLS CUI [2,2])
C2348867 (UMLS CUI [2,3])
C1518681 (UMLS CUI [3,1])
C1516048 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Criteria Fulfill
Item
subjects with any of the following criteria must not be enrolled in the study:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Hypersensitivity Capsaicin
Item
1. subjects with history of hypersensitivity to capsaicin.
boolean
C0020517 (UMLS CUI [1,1])
C0006931 (UMLS CUI [1,2])
Skin lesion Knee Involved
Item
2. subjects with skin lesion at the index knee.
boolean
C0037284 (UMLS CUI [1,1])
C0022742 (UMLS CUI [1,2])
C1314939 (UMLS CUI [1,3])
Surgical procedure on lower extremity
Item
3. a history of lower extremity surgery within 6 months prior to screening v0.
boolean
C0187763 (UMLS CUI [1])
Injury Knee Involved
Item
4. significant prior injury to the index knee within 12 months prior to screening v0.
boolean
C3263723 (UMLS CUI [1,1])
C0022742 (UMLS CUI [1,2])
C1314939 (UMLS CUI [1,3])
Spinal Disease Affecting Knee Involved | Disease Lower extremity joint Affecting Knee Involved
Item
5. disease of the spine or other lower extremity joints of sufficient degree to affect the index knee.
boolean
C0037933 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0022742 (UMLS CUI [1,3])
C1314939 (UMLS CUI [1,4])
C0012634 (UMLS CUI [2,1])
C0584731 (UMLS CUI [2,2])
C0392760 (UMLS CUI [2,3])
C0022742 (UMLS CUI [2,4])
C1314939 (UMLS CUI [2,5])
Pharmaceutical Preparations Affecting Bone metabolism | Pharmaceutical Preparations Affecting Cartilage metabolism
Item
6. 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])
CORTICOSTEROIDS FOR SYSTEMIC USE chronic
Item
chronic systematic corticosteroids
boolean
C3653708 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
Hyaluronan Injection Knee Involved
Item
hyaluronan injection into the index knee with in the previous 6 months.
boolean
C0020196 (UMLS CUI [1,1])
C1828121 (UMLS CUI [1,2])
C0022742 (UMLS CUI [1,3])
C1314939 (UMLS CUI [1,4])
diacetylrhein
Item
diacerin treatment within the last 12 months.
boolean
C0057678 (UMLS CUI [1])

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