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OpenTrials
Completed

NCT Number: NCT01039571

Single Versus Double Row Suture Anchor Repair in Medium to Large Rotator Cuff Tears

The purpose of this study is to determine whether double row repair is better in healing than traditional single row repair in arthroscopic rotator cuff repair.

Our null hypothesis is there are no differences in clinical and structural results

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Samsung Medical Center

Seoul, 135-710, South Korea

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Rotator cuff tears
  • tear size between 2cm~4cm

Exclusion criteria

  • Subscapularis tear requiring repair
  • open repair
  • any prior history of surgery on the affected shoulder
  • any fracture history around shoulder girdle(clavicle, humerus, acromion)
  • glenohumeral joint arthritis
  • inflammatory arthropathy

Treatment and study plan

double row repair

Procedure

double row repair for torn rotator cuff were performed to compare with the conventional single row repair

Other names: dual row repair

Primary outcomes

  1. Retear rate in each group(single row repair group and double row repair group)

    Time frame: MRI after 6 months from surgery

Sponsors and collaborators

Lead sponsor

Samsung Medical Center

Other

Registry information

Official study title

Prospective Randomized Case-controlled Blinded Study of Single Versus Double Row Suture Anchor Repair in Medium to Large Rotator Cuff Tears

Important dates

Study start
2005
Primary completion
2010
Study completion
2010
First posted
Dec 25, 2009
Registry last updated
Apr 22, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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