ID

42582

Beschrijving

Assessing the Impact of Isokinetic Muscular Strengthening in Eccentric Mode in the Medical Treatment of Knee Osteoarthritis; ODM derived from: https://clinicaltrials.gov/show/NCT01586130

Link

https://clinicaltrials.gov/show/NCT01586130

Trefwoorden

Versies (1)
  1. 15-09-21 15-09-21 -
Houder van rechten

University Hospital, Clermont-Ferrand

Geüploaded op

15 september 2021

DOI

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Licentie

Creative Commons BY-NC 4.0
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Eligibility Unilateral Knee Osteoarthritis NCT01586130

Engels

Eligibility Unilateral Knee Osteoarthritis NCT01586130

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient male or female, age ranging from 40 to 70 years old
Beschrijving

Gender | Age

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
patient suffering from one-sided knee o.a. regarding criteria of the american college of rheumatology (a.c.r.), with radiologic score ranging from 2 to 3 according to the kellgren & lawrence classification.
Beschrijving

One-sided knee osteoarthritis | American College of Rheumatology Improvement Criteria | Kellgren & Lawrence classification

Datatype

boolean

Alias
UMLS CUI [1,1]
C0409959
UMLS CUI [1,2]
C0205092
UMLS CUI [2]
C3273747
UMLS CUI [3]
C3177117
patient receiving medical support
Beschrijving

Medical support

Datatype

boolean

Alias
UMLS CUI [1,1]
C0344211
UMLS CUI [1,2]
C0205476
patient that did not receive any infiltration on knee within two months before randomisation.
Beschrijving

Absence of recent infiltration on knee

Datatype

boolean

Alias
UMLS CUI [1,1]
C0022742
UMLS CUI [1,2]
C0702249
UMLS CUI [1,3]
C0332185
UMLS CUI [1,4]
C0332197
patient free from any disease that could be a contraindication to the study treatment
Beschrijving

Absence of contraindication to the clinical trial

Datatype

boolean

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C1301624
UMLS CUI [1,3]
C0332197
patient able to understand the protocol and willing to comply with its rules.
Beschrijving

Compliance behavior

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
patient willing to give consent.
Beschrijving

Informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
patient affiliated to the french social secu
Beschrijving

Patient affiliated to the french social secu

Datatype

boolean

Alias
UMLS CUI [1,1]
C1510826
UMLS CUI [1,2]
C0037435
UMLS CUI [1,3]
C1556084
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient carrying prosthesis.
Beschrijving

Patient carrying prosthesis

Datatype

boolean

Alias
UMLS CUI [1,1]
C0175649
UMLS CUI [1,2]
C0206243
patient suffering from inflammatory arthritis, or flare of arthritis.
Beschrijving

Inflammatory arthritis | Flare of arthritis

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003864
UMLS CUI [1,2]
C0333348
UMLS CUI [2]
C0857103
patient suffering from symptomatic patellofemoral osteoarthritis.
Beschrijving

Symptomatic patellofemoral osteoarthritis

Datatype

boolean

Alias
UMLS CUI [1,1]
C1542808
UMLS CUI [1,2]
C0231220
patient suffering from cardio-vascular or pneumologic disease that could a contraindication to the study treatment.
Beschrijving

Cardiovascular disease as a contraindication | Lung disease as a contraindication

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0007222
UMLS CUI [1,3]
C0008976
UMLS CUI [1,4]
C0522473
UMLS CUI [2,1]
C0009488
UMLS CUI [2,2]
C0024115
UMLS CUI [2,3]
C0008976
UMLS CUI [2,4]
C0522473
patient suffering from any pathology that could cause muscular weakness (myopathy, neuropathy, hemiplegia...)
Beschrijving

Pathology that could cause muscular weakness

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030664
UMLS CUI [1,2]
C0678227
UMLS CUI [1,3]
C0151786
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Similar models

Eligibility Unilateral Knee Osteoarthritis NCT01586130

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Age
Item
patient male or female, age ranging from 40 to 70 years old
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
One-sided knee osteoarthritis | American College of Rheumatology Improvement Criteria | Kellgren & Lawrence classification
Item
patient suffering from one-sided knee o.a. regarding criteria of the american college of rheumatology (a.c.r.), with radiologic score ranging from 2 to 3 according to the kellgren & lawrence classification.
boolean
C0409959 (UMLS CUI [1,1])
C0205092 (UMLS CUI [1,2])
C3273747 (UMLS CUI [2])
C3177117 (UMLS CUI [3])
Medical support
Item
patient receiving medical support
boolean
C0344211 (UMLS CUI [1,1])
C0205476 (UMLS CUI [1,2])
Absence of recent infiltration on knee
Item
patient that did not receive any infiltration on knee within two months before randomisation.
boolean
C0022742 (UMLS CUI [1,1])
C0702249 (UMLS CUI [1,2])
C0332185 (UMLS CUI [1,3])
C0332197 (UMLS CUI [1,4])
Absence of contraindication to the clinical trial
Item
patient free from any disease that could be a contraindication to the study treatment
boolean
C0008976 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Compliance behavior
Item
patient able to understand the protocol and willing to comply with its rules.
boolean
C1321605 (UMLS CUI [1])
Informed consent
Item
patient willing to give consent.
boolean
C0021430 (UMLS CUI [1])
Patient affiliated to the french social secu
Item
patient affiliated to the french social secu
boolean
C1510826 (UMLS CUI [1,1])
C0037435 (UMLS CUI [1,2])
C1556084 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Patient carrying prosthesis
Item
patient carrying prosthesis.
boolean
C0175649 (UMLS CUI [1,1])
C0206243 (UMLS CUI [1,2])
Inflammatory arthritis | Flare of arthritis
Item
patient suffering from inflammatory arthritis, or flare of arthritis.
boolean
C0003864 (UMLS CUI [1,1])
C0333348 (UMLS CUI [1,2])
C0857103 (UMLS CUI [2])
Symptomatic patellofemoral osteoarthritis
Item
patient suffering from symptomatic patellofemoral osteoarthritis.
boolean
C1542808 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
Cardiovascular disease as a contraindication | Lung disease as a contraindication
Item
patient suffering from cardio-vascular or pneumologic disease that could a contraindication to the study treatment.
boolean
C0009488 (UMLS CUI [1,1])
C0007222 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0522473 (UMLS CUI [1,4])
C0009488 (UMLS CUI [2,1])
C0024115 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
C0522473 (UMLS CUI [2,4])
Pathology that could cause muscular weakness
Item
patient suffering from any pathology that could cause muscular weakness (myopathy, neuropathy, hemiplegia...)
boolean
C0030664 (UMLS CUI [1,1])
C0678227 (UMLS CUI [1,2])
C0151786 (UMLS CUI [1,3])
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