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Not yet recruitingNCT07925788LHBTUpdated Nov 9, 2026

Arthroscopy-Assisted Lower Trapezius Transfer Using Long Head of Biceps Tendon Autograft as an Interposition Graft for Massive Irreparable Rotator Cuff Tears

An interventional study of Arthroscopy-Assisted Lower Trapezius Transfer Using Long Head of Biceps Tendon Autograft as an Interposition Graft for Massive Irreparable Rotator Cuff Tears in Tendon Transfer, sponsored by Al-Azhar University. Not yet recruiting at 1 site in Egypt. Per ClinicalTrials.gov, last updated 2026-11-09.

Sponsored by Al-Azhar University · Not applicable, Interventional, and Treatment

Updated Nov 9, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
2
Allocation
Not applicable
Sex
All
01

Study summary

The aim of the study is To evaluate the clinical, functional, and radiological outcomes of arthroscopically assisted lower trapezius tendon transfer using LHBT autograft as an interposition graft for massive irreparable rotator cuff tears., in terms of pain relief, shoulder range of motion, external rotation strength, patient-reported functional scores, and structural integrity of the transfer.

Read the detailed description

Massive rotator cuff tears represent a major cause of shoulder pain and disability among middle-aged and older patients. In younger, active patients with symptomatic massive irreparable tears, joint-preserving reconstructive procedures are generally favored over arthroplasty in order to maintain native anatomy and delay the need for prosthetic replacement. Tendon transfer of latissmus dorsi is preferered with autograft like Achillis tendon or semitendonosus tendon in this study we will use Long head of biceps tendon as interposition graft and evaluate the result clinicaly radiologicaly and functionaly postoperative

02

Conditions studied

  • Tendon Transfer
03

In context

Lead sponsor

Al-Azhar University is the lead sponsor of 531 studies on the registry; 172 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • symptomatic massive posterosuperior rotator cuff tear (involving ≥2 tendons and/or ≥5 cm in the anteroposterior dimension) confirmed by MRI
  • Tear confirmed intraoperatively as irreparable despite maximal mobilization (medialized footprint repair not feasible)
  • Intact or repairable subscapularis tendon
  • Intact deltoid muscle function
  • Failure of at least 3-6 months of conservative treatment (physiotherapy, analgesics, activity modification) or prior failed rotator cuff repair
  • Preoperative active or passive forward elevation ≥ 0°-30° (i.e., not a pseudoparalytic shoulder with fixed loss of elevation, per surgeon's assessment) - to be defined per the surgical team's operative criteria
  • Available and functioning lower trapezius muscle and long head of biceps tendon on preoperative examination/imaging
  • Patient willing and able to comply with the postoperative rehabilitation protocol and scheduled follow-up visits

Exclusion criteria

Exclusion criteria :

  • Advanced glenohumeral osteoarthritis (Hamada grade ≥ 3)
  • Irreparable subscapularis tear or anterosuperior tear pattern
  • Deltoid dysfunction, paralysis, or previous deltoid detachment
  • Lower trapezius dysfunction, atrophy, or prior denervation (e.g., spinal accessory nerve injury)
  • Long head of biceps tendon absent, previously ruptured, or already tenotomized/tenodesed
  • Axillary nerve palsy or brachial plexus injury
  • Active glenohumeral or periprosthetic infection
  • Uncontrolled systemic disease precluding surgery (e.g., uncontrolled diabetes mellitus, severe cardiopulmonary disease)
  • Inflammatory arthropathy of the shoulder
  • Previous ipsilateral shoulder arthroplasty
  • Patients unable or unwilling to give or to comply with follow-up
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

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You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
2 participants (estimated)

Study arms

  • Experimental
    Long head of biceps tendon autograft

    We asses the outcomes of Arthroscopy-Assisted Lower Trapezius Transfer Using Long Head of Biceps Tendon Autograft as an Interposition Graft for Massive Irreparable Rotator Cuff Tears

    Procedure: Arthroscopy-Assisted Lower Trapezius Transfer Using Long Head of Biceps Tendon Autograft as an Interposition Graft for Massive Irreparable Rotator Cuff Tears

Interventions

  • ProcedureArthroscopy-Assisted Lower Trapezius Transfer Using Long Head of Biceps Tendon Autograft as an Interposition Graft for Massive Irreparable Rotator Cuff Tears

    Arthroscopy-Assisted Lower Trapezius Transfer Using Long Head of Biceps Tendon Autograft as an Interposition Graft for Massive Irreparable Rotator Cuff Tears

06

What researchers measure

Primary outcomes

  1. change in Constant-Murley Shoulder Score

    The Constant-Murley Shoulder Score (CMS) is a 100-point combined subjective and objective scoring system designed to assess overall shoulder function: Maximum Score: 100 points (indicates best possible shoulder function) Minimum Score: 0 points (indicates severe limitation/impairment)

    Time frame: 6 weeks, 3, 6,9,months and 1 year

Secondary outcomes

  1. Visual analog score VAS

    psychometric response scale used to measure subjective pain intensity, including shoulder pain: Standard Format: A 10 cm (100 mm) horizontal line anchored by two extreme descriptors at each end: 0 cm (0 mm): "No pain" 10 cm (100 mm): "Worst imaginable pain" (or "Worst pain ever felt")

    Time frame: 6 weeks, 3, 6,9,months and 1 year

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided — Data will be available with a corresponding offer on reasonable request

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Nov 2026; primary completion for Nov 2027, 12 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 4, 2026
First posted
Nov 9, 2026
StartEst.
Nov 15, 2026
Primary completionEst.
Nov 15, 2027
CompletionEst.
Nov 15, 2028
Last update
Nov 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 9, 2026
Show all 1 update
  1. Nov 9, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07925788
Responsible party
Mahmoud Mohamed Sayed Mahran (Specialist, Al-Azhar University) — Principal investigator
First posted
Nov 9, 2026
Start date
Nov 15, 2026 (estimated)
Primary completion
Nov 15, 2027 (estimated)
Completion
Nov 15, 2028 (estimated)
Last update
Nov 9, 2026

Study contacts

Mahmoud M S Mahran, MD
Contact
mahmoudmahran408@gmail.com
00201018882565
Esraa S Kotb, Master
Contact
Esraasayed845@gmail.com
01009595394

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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