Tight Management for Rotator Cuff Tendinopathy
Tight Control for Rotator Cuff Tendinopathy
Recruiting
N/A
Interventional Study
Rotator Cuff Tendinopathy
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 156 (estimated)
- Sponsor
- Nantes University Hospital · Other
Who this trial is looking for
This trial is looking for adults with new shoulder pain from rotator cuff tendinopathy. Participants will receive more frequent check-ins with a doctor to help improve their condition faster than standard care.
Are You a Good Fit for This Trial?
You may be able to join if
- I have shoulder pain that started less than 6 months ago
- I am between 18 and 65 years old
- I have pain on activity rated at least 4 out of 10
- My pain matches the symptoms of rotator cuff tendinopathy
You may not be able to join if
- I cannot have steroid injections
- I have shoulder pain from trauma such as dislocation or fracture
- I have already had a steroid injection for my shoulder in this episode
- I have neurological issues affecting my shoulder
- I have other shoulder problems like arthritis or frozen shoulder
- I have a tendon calcification larger than 0.5 cm
- I have had shoulder surgery before
- I have a full-thickness tear of a tendon
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
The main objective of the study is to determine whether tight management of patients in early rotator cuff tendinopathy would lead to better clinical improvement than standard management. In a randomized study, we propose to compare two types of management, with a tight control group having one consultation per month for the first 3 months, in order to readapt or intensify management, whereas the …
Trial Locations
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Eligibility Criteria
Inclusion Criteria :
Patient with new-onset shoulder pain related to rotator cuff tendinopathy
* Age between 18 and 65
* Shoulder pain on activity for less than 6 months with VAS≥4/10 and/or OSS≥20
* Pain compatible with rotator cuff tendinopathy according to the rotator cuff tendinopathy accordin…
Contacts