Study on the Application of Shock Wave Technique After Rotator Cuff Operation
NCT06563739 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70
Last updated 2024-08-21
Summary
This study is a prospective cohort study and is a single-center clinical trial. The subjects of this study were patients who underwent rotator cuff repair in the Department of Sports Medicine and the Department of Rehabilitation in the Third Hospital of Beijing Medical University. The sample size of this study is about 2600 cases. We will collect the results of shoulder joint function score, quality of life score, pain score and MRI examination of all participants at baseline. Meanwhile, epidemiological data and related clinical characteristics of patients will be collected at the time of enrollment. All the collected data information was entered into the computer for statistical analysis, and the prognosis of patients under different programs was evaluated.
Conditions
- Rotator Cuff Tear
Interventions
- PROCEDURE
-
Divergent low energy shock wave
Receive divergent low energy shock wave once a week
- PROCEDURE
-
Divergent low energy shock wave
Receive divergent low energy shock wave twice a week
- PROCEDURE
-
Divergent medium and low energy shock wave
Receive divergent medium and low energy shock wave once a week
- PROCEDURE
-
Divergent medium and low energy shock wave
Receive divergent medium and low energy shock wave twice a week
- PROCEDURE
-
Focused low energy shock wave
Receive focused low energy shock wave once a week
- PROCEDURE
-
Divergent medium energy shock wave
Receive divergent medium energy shock wave once a week
- PROCEDURE
-
Divergent medium energy shock wave
Receive divergent medium energy shock wave twice a week
- PROCEDURE
-
Non-exposed group
Traditional rehabilitation assessment and training guidance
Sponsors & Collaborators
-
Peking University Third Hospital
lead OTHER
Principal Investigators
-
Guoqing Cui · Peking University Third Hospital
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-05-05
- Primary Completion
- 2024-12-30
- Completion
- 2024-12-30
Countries
- China
Study Locations
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