Perianchor Cyst Formation, Tendon Healing, and Clinical Outcomes Following Arthroscopic Rotator Cuff Repair

NCT07661680 · tracked via the Priya Life Science Turkey tracker

Sponsor

Fatih Sultan Mehmet Training and Research Hospital

Phase

Observational

Started

2026-05-01

Last updated

2026-09-09

Condition(s) studied

Rotator Cuff TearsTendon ThickeningTendon InjuriesMuscle Weakness

Investigational drug(s) / intervention(s)

MRI

MRI: Measure of Perianchor Cyst Formation using 3D Slicer Image Computing Platform

Study summary

Perianchor cyst formation is frequently observed after arthroscopic rotator cuff repair; however, its clinical significance remains unclear. This study aims to evaluate the relationship between anchor-related parameters and cyst formation, as well as their association with tendon healing and functional outcomes.

Eligibility

Sex

ALL

Min age

18 Years

Max age

70 Years

Healthy volunteers

Inclusion Criteria: * Age 18-70 years * Undergoing primary arthoroscopic rotator cuff repair * Availability for MRI follow-up * Ability to provide informed constent Exclusion Criteria: * Previous shoulder surgery * Active infection * Inflammatory joint disease * Acute traumatic massive tears * Inability to complete follow-up

Primary outcome measure(s)

Perianchor Cyst Volume — Up to 12 months
To determine the effect of anchor-related surgical parameters on peri-anchor cyst volume.
Deadman's Angle — Up to 12 months
Relation between anchors angle and cyst volume

Trial sites (1)

Facility	City	Region	Status
Istanbul Provincial Health Directorate Fatih Sultan Mehmet Training and Research Hospital	Istanbul	Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07661680 on ClinicalTrials.gov ↗ ← All trials in Turkey