Valuation of the Dexketoprofen Effectiveness on Subacromial Syndrome With Different Physiotherapy Treatments.
Trial Snapshot
- Phase
- Phase 2
- Status
- Completed
- Sponsor
- Enrollment
- 99
- Locations
- 2
- Primary Endpoint
- Pain measure by the visual analogic scale pain score.
Study Overview
Brief Summary
The purpose of this study is to determine whether dexketoprofen administered by phonophoresis or iontophoresis is more effective in the treatment of subacromial syndrome that the conventional therapy with ultrasounds.
Detailed Description
It is a question of valuing the decrease of the pain (by means of the visual analogic scale pain score) and the increase of the functionality of the joint (by means of Dash and Constant scores) of three different treatments from physical therapy to establish the most effective protocol for the treatment of the subacromial syndrome.
Determine the best physiotherapy treatment for subacromial syndrome with 20 sessions of different treatments.
A group will receive the conventional treatment with ultrasounds without drugs, another group will receive dexketoprofen by phonophoresis and the third group will receive dexketoprofen by iontophoresis.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 36 Years to 70 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Subacromial syndrome diagnosed by ultrasound scanning with Rotator cuff tendinitis or partial break of the rotator cuff and / or of the brachial biceps.
- •Informed consent.
Exclusion Criteria
- •To suffer shoulder arthritis or any shoulder pathology with mobility limitation.
- •Fibromyalgia
- •Psychologic or psychiatric pathologies
- •Hypersensibility to the drug
- •Back or shoulder traumatism
- •To have received an analgesic infiltration on the affected shoulder in the last month
- •Lack of adherence to the treatment upper to 15 % of the sessions
Outcomes
Primary Outcomes
Pain measure by the visual analogic scale pain score.
Time Frame: 1 month
Secondary Outcomes
- Functionality of the joint by Dash and Constant scores(1 month)
Investigators
Rosa Sola
University Professor
University Rovira i Virgili