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Comparison of Trans-Osso and Anchor Suture methods in rotator cuff tears

Comparison of two transosseous and suture anchors methods in rotator cuff tears and its effect on shoulder function :A double-blind clinical trial study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240425061571N1
Enrollment
62
Registered
2025-02-13
Start date
2025-02-19
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Rotator cuff tear. Rotator cuff tear or rupture, not specified as traumatic

Interventions

Intervention 1: Intervention group: anchor suture . To perform rotator cuff repair, we use a transverse incision (instead of a longitudinal incision) with an anterolateral approach to leave less scar

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: MRI-confirmed full-thickness rotator cuff tendon tear Grade 1 and 2 Cofield classification Grade 1 and 2 Peta classification Grade 1 and 2 goutallier classification Unsuccessful conservative treatment for more than 3 months Acceptable active range of motion before surgery

Exclusion criteria

Exclusion criteria: Brachial plexopathy , neoplasm Pregnancy Diabetes Addiction to opioids Cofield classification grade 3 and above Gauthalie classification grade 3 and above History of shoulder surgery and fracture on the same side

Design outcomes

Primary

MeasureTime frame
The University of California-Los Angeles (UCLA) shoulder scale. Timepoint: Before the intervention and 3, 6, and 12 months after the intervention. Method of measurement: UCLA shoulder function scale questionnaire.

Secondary

MeasureTime frame
Disabilities of the Arm, Shoulder and Hand (DASH) upper extremity disability Scale. Timepoint: Before the intervention and 3, 6, and 12 months after the intervention. Method of measurement: DASH Upper Extremity Disability Questionnaire.;Visual Analogue Scale (VAS). Timepoint: 6 hours after surgery. Method of measurement: Visual Analog Scale Questionnaire.;Complications of infection after surgery. Timepoint: 3 months after surgery. Method of measurement: Elevated leukocytes in blood tests.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactYasin Sharifzadeh

Babol University of Medical Sciences

dryasinsharifzadeh@gmail.com+98 11 3225 2071

Outcome results

None listed

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