Placental patch could help shoulder tears heal better
NCT ID NCT07027735
First seen Jun 25, 2026 · Last updated Sep 11, 2026 · Updated 3 times
Summary
This study tests whether a patch made from donated placental tissue can help rotator cuff tears heal better after surgery. Half of the 120 participants will get the patch along with standard repair, and the other half will get standard repair alone. An MRI one year later will check if the tendon has healed properly.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- decellularized human placental extracellular matrix allograft patch
- What this could lead to
- If it works, this patch could reduce the chance of rotator cuff tears coming back after surgery, helping more people regain full shoulder function.
- What could go wrong
- This is a mid-stage trial with 120 people, so results may not apply to everyone. The patch might not improve healing over standard surgery, and there are always surgical risks like infection or graft failure.
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
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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
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Jul 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Age ≥ 18 years * Diagnosis of full thickness rotator cuff tear Exclusion Criteria: * Partial thickness tears * Full thickness subscapularis tears * Goutallier grades 3 and 4 * Prior rotator cuff surgery
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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NewYorkPresbyterian Hospital @ Columbia University Irving Medical Center
New York, New York, 10032-3702, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a Stomach-Derived peptide help tendons heal faster after surgery?
- Can a patch make torn shoulder tendons heal stronger?
- 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