Study on the Application of Shock Wave Technique After Rotator Cuff Operation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorPeking University Third Hospital

About this trial

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.

Eligibility criteria

Qualifiers

A rotator cuff tear was diagnosed and surgery was required

Able to complete cardiopulmonary exercise tests

Able to cooperate with rehabilitation training and complete questionnaire survey

Disqualifiers

Age <17 years or age >75 years

Previous shoulder surgery history

Irreparable rotator cuff damage

Trial design

Treatments tested in this trial

  • Divergent low energy shock wave
  • Divergent low energy shock wave
  • Divergent medium and low energy shock wave
  • Divergent medium and low energy shock wave
  • Focused low energy shock wave
  • Divergent medium energy shock wave
  • Divergent medium energy shock wave
  • Non-exposed group

Treatment groups

70 Participants
are divided into 8 treatment groups

8

Treatment groups

See each treatment group below.