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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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23 May 2016 |
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Main ID: |
NCT02308514 |
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Date of registration:
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26/11/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Does Adding Cryostimulation to Conservative Care Help in Managing Chronic Lateral Epicondylitis? a Pilote Study
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Scientific title:
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Does Adding Cryostimulation to Conservative Care Help in Managing Chronic Lateral Epicondylitis? a Pilote Study |
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Date of first enrolment:
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September 2014 |
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Target sample size:
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40 |
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Recruitment status: |
Active, not recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT02308514 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Caregiver), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Canada
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Contacts
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Name:
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Nadia Richer Richer, M.Sc. |
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Address:
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Telephone:
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Email:
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Affiliation:
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Clinique universitaire de chiropratique |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Must have pain at lateral elbow (lateral epicondylitis) for at least six months
- Pain must not come from trauma
- Painful palpation of the lateral epicondyle
- At least one out of two positive test: Cozen's, Mill's
Exclusion Criteria:
- Fibromyalgia
- Diabetes
- Patient taking more than three medications at the time of inclusion
- Cervical radiculopathy
- Painful shoulder
- Cold intolerance / allergies
- Smoking
- Cortisone infiltration at the painful lateral epicondyle in the month previous to the
inclusion
Age minimum:
18 Years
Age maximum:
65 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Lateral Epicondylitis
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Intervention(s)
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Other: conservative care
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Device: cryostimulation
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Primary Outcome(s)
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Visual Analog Pain Scale
[Time Frame: at inclusion - ninth visit - 3 months after last treatment]
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Secondary Outcome(s)
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pain free grip strength
[Time Frame: at inclusion - ninth visit - 3 months after last treatment]
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Secondary ID(s)
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CER-14-203-07.08
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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