Actively Recruiting

Phase Not Applicable
Age: 20Years - 60Years
All Genders
NCT05792202

Combined Microfracture Procedure Promotes Tendon Healing

Led by Beijing Jishuitan Hospital · Updated on 2024-04-29

50

Participants Needed

1

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is a prospective randomized controlled study of Combined microfracture procedure promotes tendon healing during double raw repair for full tear rotator cuff. The patients with rotator cuff tear were randomly divided into groups before the operation. The patients were followed up before and 6 weeks, 3 months, 6 months, 12 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 Crimson duvet procedure with Greenhouse procedure on the treatment of rotator cuff.

CONDITIONS

Official Title

Combined Microfracture Procedure Promotes Tendon Healing

Who Can Participate

Age: 20Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

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Trial Site Locations

Total: 1 location

1

Beijing Jishuitan hospital

Beijing, Beijing Municipality, China, 100000

Actively Recruiting

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Research Team

S

Shangzhe Li, M.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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