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Tendon Transfer Rotator Cuff Tear

University of Maryland Baltimore (UMB) logo

University of Maryland Baltimore (UMB)

Status

Terminated

Conditions

Rotator Cuff Tears

Treatments

Procedure: Latissimus Dorsi Tendon Transfer Technique
Procedure: Pectoralis Tendon Transfer Technique
Procedure: Lower Trapezius Tendon Transfer Technique

Study type

Interventional

Funder types

Other

Identifiers

NCT04588506
HP-00091132

Details and patient eligibility

About

This is a prospective randomized study on using muscle tendons to repair tears of the muscles on the shoulder. There are 3 muscles covering the shoulder joint- supraspinatus, infraspinatus and subscapularis. Large tears involving these muscles can be treated by using some muscle from another location of the body known as Tendon transfer techniques. These muscle tendons may be from the lower back (Latissimus Dorsi), upper pack (lower trapezius) or chest (pectoralis). There are currently no studies to show which tendon transfer technique has better outcomes.

This study comprises two trials and a total of 84 participants would be enrolled. Each trial comparing the patient reported outcomes between two tendon transfer techniques. Large tears involving the supraspinatus and infraspinatus would be repaired using either the Latissimus dorsi technique or Lower trapezius technique. 21 patients would be randomly assigned to either groups. The second trial would be comparing the Latissimus dorsi technique and pectoralis technique in large tears of the subscapularis muscle. Another 21 patients would be randomly assigned to either groups.

The investigators are studying to see if the Lower Trapezius and Pectoralis transfer techniques for muscle tear repairs would have better post-surgical outcomes compared with Latissimus Dorsi transfer technique.

For both trials, participants would be followed up for 2 years and post-surgical outcomes would be compared between treatment groups.

Enrollment

10 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects must have massive, irreparable tear of the posterior-superior rotator cuff
  • Subjects between 18 years and 65 years (≥ 18 and ≤ 65 years of age).
  • Diagnosis of no to minimal glenohumeral arthritis- Hamada 1 and 2
  • Subject with irreparable subscapularis tendon tear (Arms 3 and 4 ONLY)

Exclusion criteria

  • Subjects having severe glenohumeral arthritis
  • History of prior tendon transfer
  • Axillary nerve injury
  • Deltoid deficiency
  • Subjects with pseudo paralysis
  • History of post-operative deep shoulder infection
  • Non-English-speaking subjects.
  • Subject has any condition, that in the opinion of the investigator, would prevent them from completing this study
  • Subject with irreparable subscapularis tendon tear (Arms 1 and 2 ONLY)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

10 participants in 4 patient groups

Cuff tear without subscapularis tear-Lower Trapezius group
Active Comparator group
Description:
Rotator cuff tears excluding the subscapularis muscle repaired using Lower Trapezius tendon
Treatment:
Procedure: Lower Trapezius Tendon Transfer Technique
Cuff tear without subscapularis tear-Latissimus Dorsi group
Active Comparator group
Description:
Rotator cuff tears excluding the subscapularis muscle repaired using Latissimus Dorsi tendon
Treatment:
Procedure: Latissimus Dorsi Tendon Transfer Technique
Cuff tear involving subscapularis tear-Pectoralis group
Active Comparator group
Description:
Rotator cuff tears involving the subscapularis muscle repaired using Pectoralis tendon
Treatment:
Procedure: Pectoralis Tendon Transfer Technique
Cuff tear involving subscapularis tear-Latissimus Dorsi group
Active Comparator group
Description:
Rotator cuff tears involving the subscapularis muscle repaired using Latissimus Dorsi tendon
Treatment:
Procedure: Latissimus Dorsi Tendon Transfer Technique

Trial contacts and locations

1

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Central trial contact

Ashfaq S Hasan, MD

Data sourced from clinicaltrials.gov

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