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Cutting-through at the Greater Tuberosity

C

Chuncheon Sacred Heart Hospital

Status

Completed

Conditions

Rotator Cuff Tears

Treatments

Procedure: Arthroscopic suture-bridge rotator cuff repair

Study type

Observational

Funder types

Other

Identifiers

NCT04587180
2014-33

Details and patient eligibility

About

The investigators evaluated the correlation between cutting-through at the greater tuberosity (GT) just medial to the lateral knotless anchor in arthroscopic suture-bridge rotator cuff repair and the bone mineral density (BMD) of the lumbar spine, hip and GT of the proximal humerus and to evaluate factors and clinical outcomes related to cutting-through at the GT.

Full description

Seventy-eight patients who underwent arthroscopic suture-bridge rotator cuff repair and who had undergone dual energy X-ray absorptiometry (DEXA) scans before surgery were included. Patients were divided into two groups: patients who had cutting-through (46, group I) and patients who did not (32, group II). Clinical and radiological data including demographics, BMDs, fatty infiltration of rotator cuff muscles, tear size, tear involvement, VAS pain score, and ASES score were analyzed.

Enrollment

95 patients

Sex

All

Ages

50 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Primary arthroscopic repair for a symptomatic full-thickness rotator cuff tear identified by preoperative MRI
  2. Dual energy X-ray absorptiometry (DEXA) to evaluate the BMD of the lumbar spine and hip, as a standardized measurement, and the GT of the affected proximal humerus
  3. Follow up for a minimum of 2 years after the primary surgery.

Exclusion criteria

  1. Primary arthroscopic repair due to partial-thickness rotator cuff tear or an isolated subscapularis tear
  2. Primary suture-bridge repair with 3 or more lateral-knotless anchors
  3. Previous history of fractures or surgeries on the affected shoulder
  4. Shoulder instability
  5. Glenohumeral osteoarthritis
  6. Neurologic or systemic disease diseases influencing the shoulder joint 7 History of infection of the shoulder joint

Trial design

95 participants in 2 patient groups

Patients with cutting-through
Description:
Patients who had cutting-through during the lateral knotless anchor fixation.
Treatment:
Procedure: Arthroscopic suture-bridge rotator cuff repair
Patients without cutting-through
Description:
Patients who didn't have cutting-through during the lateral knotless anchor fixation.
Treatment:
Procedure: Arthroscopic suture-bridge rotator cuff repair

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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