Informações:
Falhas:
ID
31274
Descrição
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
Palavras-chave
Versões (1)
- 06/08/2018 06/08/2018 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
6 de agosto de 2018
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Osteoarthritis NCT00712816
Eligibility Osteoarthritis NCT00712816
- StudyEvent: Eligibility
Similar models
Eligibility Osteoarthritis NCT00712816
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
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])
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])
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])
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])
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])
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])
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])
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])