Does Medial Raw Anchor Necessary During Tendon Repair Combined With Microfracture

Beijing Jishuitan Hospital

Status: Invitation-only

Conditions: Full Rotator Cuff Tear; Microfracture Procedure; Double Raw Repair; Lateral Raw Repair

Treatments: Procedure: lateral raw; Procedure: double raw

Study type: Interventional

Funder types: Other

Identifiers

NCT06431191

luyi

Details and patient eligibility

About

This study is a prospective randomized controlled study of rotator cuff repair with lateral raw or double raw combined with microfracture procedure. The patients with rotator cuff tear were randomly divided into groups before the operation. The patients were followed up before and, 3 months, 6 months, 12 months and 24 months after surgery. In different time periods, the quantitative and qualitative indicators including pain, functional score, muscle strength, MRI performance, etc. were compared between groups at the same time period to evaluate the difference in the effect of double raw or only lateral raw repair combined with microfracture on the treatment of rotator cuff. In order to figure out whether medial raw anchor necessary during tendon repair combined with microfracture in small to medium size rotator cuff tear.

Enrollment: 50 estimated patients

Sex: All

Ages: 20 to 60 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Arthroscopy confirmed small to medium full rotator cuff tear
• Unilateral rotator cuff injury
• Voluntarily accept randomized controlled grouping, cooperate with treatment and follow up patients
• Young and middle-aged patients aged 20 to 60

Exclusion criteria

• Previous shoulder surgery (incision or arthroscopy)
• Combined with diseases of other parts of the same limb
• Combined with Bankart injury, acromioclavicular joint disease, greater tuberosity fracture, glenoid fracture and so on
• Bilateral onset
• Unable or unwilling to receive clinical follow-up

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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50 participants in 2 patient groups, including a placebo group

Study group

Experimental group

Description:

lateral raw repair for full tear rotator cuff combined microfracture procedure

Treatment:

Procedure: lateral raw

Control group

Placebo Comparator group

Description:

double raw repair for full tear rotator cuff combined microfracture procedure

Treatment:

Procedure: double raw