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

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06563739 on ClinicalTrials.gov