New shoulder surgery technique could save money and improve recovery
NCT ID NCT07327437
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new, less expensive surgical technique called the 'Grand-Knot' for repairing full-thickness rotator cuff tears in the shoulder. 160 patients aged 45-75 were randomly assigned to get either the new technique or the standard anchor repair. Researchers measured shoulder function, pain, and tendon healing over at least 2.5 years to see which method works better.
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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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160 people
The number who actually took part.
- Started
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Jan 2021
- Finished
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Jul 2025
- 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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45 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients aged 45 to 75 years. Diagnosis of full-thickness supraspinatus or posterosuperior rotator-cuff tears. Tears suitable for arthroscopic repair. Confirmation of diagnosis and tear morphology via standardized clinical examination and MRI. Willingness to comply with a 2.5-year follow-up protocol and standardized rehabilitation. Exclusion Criteria: * Partial-thickness tears or isolated subscapularis tears. Advanced fatty infiltration (Fuchs grade 3-4). Rotator cuff arthropathy (Hamada classification \> 2). Presence of calcific tendinitis in the affected shoulder. Prior ipsilateral shoulder surgery. General medical contraindications to arthroscopy or general anesthesia. Inability to complete the follow-up or provide informed consent.
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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
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Cairo University Hospitals (Kasr Al-Ainy)
Cairo, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- 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