Skip the sling? new study tests faster rehab after shoulder surgery
NCT ID NCT03913611
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares two recovery programs after rotator cuff repair surgery. One group follows standard care—wearing a sling for 6 weeks with limited movement. The other group starts moving sooner, guided by comfort rather than strict restrictions. Researchers will measure shoulder function and use MRI scans to check if the repair holds up. The goal is to see if a faster rehab approach can improve recovery without harming healing.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- rehabilitation protocol (accelerated vs standard)
- What this could lead to
- If accelerated rehab works as well or better, patients may recover shoulder function faster and with less inconvenience after rotator cuff surgery.
- What could go wrong
- This is a small, early-stage trial with only 50 participants. Accelerated rehab might increase the risk of the repair failing or not healing properly.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
50 people
The number who actually took part.
- Started
-
Oct 2019
- Expected to finish
-
Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
40 to 80 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged over 40 with a degenerate full-thickness posterosuperior rotator cuff tear undergoing arthroscopic rotator cuff repair (+/- concomitant procedures such as biceps tenotomy and subacromial decompression). Exclusion Criteria: * Other musculoskeletal disease affecting same limb * Massive rotator cuff tear * Subscapularis tear * Incomplete cuff repair * Repair under tension * Non-English speaker * Inability to follow postoperative instructions / restrictions
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Manchester University Foundation NHS Trust
Manchester, M23 9LT, United Kingdom
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Blood-derived injections may mend torn shoulder tendons without surgery
- Ultrasound 'Tissue Stiffness' test could reveal hidden rotator cuff healing problems
- Which painkiller wins for shoulder surgery? a Head-to-Head test
- Which shoulder repair works best for massive tears? a trial pits two techniques Head-to-Head