Skip to content

Clinical outcome comparison between Arthroscopic complete RC repair and complete RC repair with biceps re-routing(BR) for rotator cuff tear

Clinical outcome comparison between Arthroscopic complete RC repair and complete RC repair with biceps re-routing(BR) for rotator cuff tear

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004456
Enrollment
120
Registered
2019-11-21
Start date
2019-01-08
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

None listed

Interventions

Procedure/Surgery : Among patients with rotator cuff tears, patients who have had a rupture based on their past history, medical history, physical examination, and MRI findings are selected. (Accordin
s consent before surgery. The surgical method is the same for both group using the anterior and posterior portal. The patient is placed in the lateral position with a posterior portal 2 cm inferior an

Sponsors

The Catholic University of Korea, Seoul St. Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria 1) Adults over 20 years of age (However, adults over 70 years of age should understand the contents of this study and participate only if they can voluntarily agree.) 2) Patient diagnosed with rotator cuff tear by MRI and physical examination 3) Those who decided to undergo arthroscopic rotator cuff repair because the symptoms persist after conservative treatment for more than 3 months 4) Patients whose rotator cuff tear is full reduction to footprint

Exclusion criteria

Exclusion criteria: Exclusion Criteria 1) A person with previous trauma or surgery of the ipsilateral shoulder 2) Arthritis of the ipsilateral glenohumeral joints 3) Those who do not want to participate in this study 4) Persons with joint stiffness: Forward flexion less than 100 degrees, or less than 30 degrees of external rotation, or less than 1st lumbar spine of internal rotation.

Design outcomes

Primary

MeasureTime frame
Shooulder Functional score (ASES score, Constant score, Korean shoulder score)

Secondary

MeasureTime frame
VAS pain score

Countries

Korea, Republic of

Contacts

Public ContactHyungjoon Kim

The Catholic University of Korea, Seoul St. Mary's Hospital

khjsdsd@gmail.com+82-2-2258-6359

Outcome results

None listed

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