ID

31274

Description

Use of Cold and Compression Therapy With Total Knee Replacement Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00712816

Link

https://clinicaltrials.gov/show/NCT00712816

Keywords

Versions (1)
  1. 8/6/18 8/6/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

August 6, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Osteoarthritis NCT00712816

English

Eligibility Osteoarthritis NCT00712816

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
at least 18 but no more than 85 years of age
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
body mass index not greater than 40
Description

Body mass index

Data type

boolean

Alias
UMLS CUI [1]
C1305855
diagnosis of osteoarthritis of the knee
Description

Osteoarthritis, Knee

Data type

boolean

Alias
UMLS CUI [1]
C0409959
medically cleared for total knee replacement surgery
Description

Total Knee Replacement Scheduled

Data type

boolean

Alias
UMLS CUI [1,1]
C0086511
UMLS CUI [1,2]
C0205539
physically and mentally able and willing to participate in and follow the study protocol and schedule
Description

Protocol Compliance

Data type

boolean

Alias
UMLS CUI [1]
C0525058
able and willing to have all postoperative physical therapy visits in a physical therapy clinic associated with the research site
Description

Physical therapy Postoperative Able | Physical therapy Postoperative Willing

Data type

boolean

Alias
UMLS CUI [1,1]
C0949766
UMLS CUI [1,2]
C0032790
UMLS CUI [1,3]
C0085732
UMLS CUI [2,1]
C0949766
UMLS CUI [2,2]
C0032790
UMLS CUI [2,3]
C0600109
signed informed consent document for the study
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
rheumatoid arthritis
Description

Rheumatoid Arthritis

Data type

boolean

Alias
UMLS CUI [1]
C0003873
severe pitting edema in the ipsilateral limb
Description

Pitting edema Severe Limb Ipsilateral

Data type

boolean

Alias
UMLS CUI [1,1]
C0333243
UMLS CUI [1,2]
C0205082
UMLS CUI [1,3]
C0015385
UMLS CUI [1,4]
C0441989
history of thrombophlebitis in lower extremities
Description

Thrombophlebitis of lower extremities

Data type

boolean

Alias
UMLS CUI [1]
C0265053
an active systemic disease such as aids, hiv, hepatitis, etc.
Description

Systemic disease | Acquired Immunodeficiency Syndrome | HIV Infection | Hepatitis

Data type

boolean

Alias
UMLS CUI [1]
C0442893
UMLS CUI [2]
C0001175
UMLS CUI [3]
C0019693
UMLS CUI [4]
C0019158
is immunologically suppressed or has received or is receiving steroids at any dose daily for more than one month within the last 12 months
Description

Therapeutic immunosuppression | Steroids Daily Dose

Data type

boolean

Alias
UMLS CUI [1]
C0021079
UMLS CUI [2,1]
C0038317
UMLS CUI [2,2]
C2348070
is pregnant or planning to become pregnant during the study period
Description

Pregnancy | Pregnancy, Planned

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
any condition that would contraindicate using the game ready
Description

Other Coding

Data type

boolean

Alias
UMLS CUI [1]
C3846158
currently enrolled in another clinical trial that could affect outcome of this study
Description

Study Subject Participation Status Affecting Research results

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0683954
previously enrolled in this study
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Osteoarthritis NCT00712816

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
at least 18 but no more than 85 years of age
boolean
C0001779 (UMLS CUI [1])
Body mass index
Item
body mass index not greater than 40
boolean
C1305855 (UMLS CUI [1])
Osteoarthritis, Knee
Item
diagnosis of osteoarthritis of the knee
boolean
C0409959 (UMLS CUI [1])
Total Knee Replacement Scheduled
Item
medically cleared for total knee replacement surgery
boolean
C0086511 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
Protocol Compliance
Item
physically and mentally able and willing to participate in and follow the study protocol and schedule
boolean
C0525058 (UMLS CUI [1])
Physical therapy Postoperative Able | Physical therapy Postoperative Willing
Item
able and willing to have all postoperative physical therapy visits in a physical therapy clinic associated with the research site
boolean
C0949766 (UMLS CUI [1,1])
C0032790 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
C0949766 (UMLS CUI [2,1])
C0032790 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Informed Consent
Item
signed informed consent document for the study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Rheumatoid Arthritis
Item
rheumatoid arthritis
boolean
C0003873 (UMLS CUI [1])
Pitting edema Severe Limb Ipsilateral
Item
severe pitting edema in the ipsilateral limb
boolean
C0333243 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0015385 (UMLS CUI [1,3])
C0441989 (UMLS CUI [1,4])
Thrombophlebitis of lower extremities
Item
history of thrombophlebitis in lower extremities
boolean
C0265053 (UMLS CUI [1])
Systemic disease | Acquired Immunodeficiency Syndrome | HIV Infection | Hepatitis
Item
an active systemic disease such as aids, hiv, hepatitis, etc.
boolean
C0442893 (UMLS CUI [1])
C0001175 (UMLS CUI [2])
C0019693 (UMLS CUI [3])
C0019158 (UMLS CUI [4])
Therapeutic immunosuppression | Steroids Daily Dose
Item
is immunologically suppressed or has received or is receiving steroids at any dose daily for more than one month within the last 12 months
boolean
C0021079 (UMLS CUI [1])
C0038317 (UMLS CUI [2,1])
C2348070 (UMLS CUI [2,2])
Pregnancy | Pregnancy, Planned
Item
is pregnant or planning to become pregnant during the study period
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Other Coding
Item
any condition that would contraindicate using the game ready
boolean
C3846158 (UMLS CUI [1])
Study Subject Participation Status Affecting Research results
Item
currently enrolled in another clinical trial that could affect outcome of this study
boolean
C2348568 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
Study Subject Participation Status
Item
previously enrolled in this study
boolean
C2348568 (UMLS CUI [1])
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