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Arthroscopic lower trapezius transfer with tendon bridging reinforcement repair in the treatment of posterosuperior massive rotator cuff tears: a single-center, single blinded randomized controlled trial.

Clinical study of arthroscopic lower trapezius transfer with tendon bridging reinforcement repair in the treatment of posterosuperior massive rotator cuff tears

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082244
Enrollment
Unknown
Registered
2024-03-25
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

posterosuperior massive rotator cuff tears

Interventions

lower trapezius transfer:arthroscopic lower trapezius transfer with tendon bridging reinforcement repair
maximum partial repair:arthroscopic maximum partial repair

Sponsors

Taizhou Hospital, Zhejiang Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. MRI confirmed posterosuperior massive rotator cuff tear (complete tear of supraspinatus and infraspinatus); 2. Adult patients (18-70 years old); 3. Pain and dysfunction severely affect daily life; 4. Conservative treatment failed; 5. Goutallier grade of fatty infiltration in infraspinatus muscle =3; 6. Warner grade of subaspinatus atrophy = moderate; 7. Hamada grade of rotator cuff joint disease =4.

Exclusion criteria

Exclusion criteria: 1. Complete repair surgery is feasible; 2. Uncontrolled diabetes (HBA1c > 7%); 3. Pregnant women; 4. Local or systemic infection exists; 5. Had received local non-vascular interventional therapy; 6. Malnutrition (albumin < 30g/L); 7. Combined with malignant tumor; 8. Combined frozen shoulder; 9. Combined with irreparable subscapular muscle tear; 10. The fat infiltration Goutallier grade of teres minor is =3; 11. Combined deltoid paralysis; 12. Combined with neurological symptoms; 13. Inability to understand or cooperate with postoperative guidance and rehabilitation; 14. Failure to provide informed consent to research.

Design outcomes

Primary

MeasureTime frame
American Shoulder and Elbow Surgeons;

Secondary

MeasureTime frame
Constant-Murley shoulder scores;University of California at Los Angeles score;visual analog scale pain score;retear;range of motivation;advance of rotator cuff joint disease;return to work time;

Countries

China

Contacts

Public ContactXiaobo Zhou

Taizhou Hospital, Zhejiang Province

dafuzhouxb@hotmail.com+86 139 5858 5383

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026