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Clinical Trials in China / NCT06431191
Enrolling by invitation Not applicable

Does Medial Raw Anchor Necessary During Tendon Repair Combined With Microfracture

NCT06431191 · tracked via the Priya Life Science China tracker
Sponsor
Beijing Jishuitan Hospital
Phase
Not applicable
Started
2023-01-01
Last updated
2024-05-28

Condition(s) studied

Full Rotator Cuff TearMicrofracture ProcedureDouble Raw RepairLateral Raw Repair

Investigational drug(s) / intervention(s)

lateral rawdouble raw

lateral raw: lateral raw repair for full tear rotator cuff combined microfracture procedure, without medial raw

double raw: double raw repair for full tear rotator cuff combined microfracture procedure

Study summary

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.

Eligibility

Sex
ALL
Min age
20 Years
Max age
60 Years
Healthy volunteers
No
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

Primary outcome measure(s)

  • rotator cuff re-tear rate — 6, 12, 24 months postoperatively
    the rotator cuff re-tear rate was measured by MRI, MRI was performed to identify the status of the tendon

Trial sites (1)

FacilityCityRegionStatus
Beijing Jishuitan hospital Beijing Beijing Municipality

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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 NCT06431191 on ClinicalTrials.gov ↗ ← All trials in China