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Effect of Extracorporeal Shock Wave Therapy After Arthroscopic Rotator Cuff Repair

Effect of Extracorporeal Shock Wave Therapy After Arthroscopic Rotator Cuff Repair

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04848103
Enrollment
30
Registered
2021-04-19
Start date
2021-05-10
Completion date
2021-07-08
Last updated
2021-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Postoperative, Rotator Cuff Injuries, Tissue Adhesion

Brief summary

Although radial extracorporeal shock wave therapy (rESWT) has proven to be an effective treatment, the effectiveness of the treatment has so far been controversial. There are no studies using rESWT in rehabilitation after arthroscopic rotator cuff repair (ARCR). Therefore, in this study, there is evidence that rESWT promotes pain control and healing recovery, and through previous studies, we would like to investigate whether treatment with rESWT during the intensive rehabilitation period of patients after ARCR is more effective in controlling pain.

Interventions

Radial extracorporeal shockwave therapy group include Therapeutic modality(Transcutaneous electrical nerve stimulation \[TENS\], Microwave thermotherapy, and Superficial heat therapy), Range of motion exercise(Continuous passive motion and Active range of motion exercise).

Sponsors

Sahmyook University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Adults over 18 years old * In case of 6 weeks after receiving arthroscopic rotator cuff repair * When the participants wishes to enroll in the study

Exclusion criteria

* 65 years old or older * If the tear area is large and augmentation is performed * If there is a previous surgical history at the surgical site * Osteoarthritis in the shoulder joint

Design outcomes

Primary

MeasureTime frameDescription
. Pain intensityChange from baseline pain intensity at 2 weeksA numeric pain rating scale (NPRS) consisting of 11 points in total from 0 points (no pain) to 10 points (the most severe pain imaginable) is used. The lower the score, the less the pain.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026