Clinical Trial

Comparative Effectiveness of Dry Cupping and Graston Techniques in Scapulocostal Syndrome.

Study acronym: CMR = Compress
Completed
View on ClinicalTrials.gov →
Summary
The goal of this clinical trial is to check the comparative effectiveness of Graston Techniques and Dry cupping in Office Workers with Scapulocostal syndrome. The main questions it aims to answer are: 1. To evaluate the relative effectiveness of dry cupping and the Graston technique. 2. How well each technique reduces symptoms and enhances work productivity and functional outcomes. 3. To assess whether integrating either Graston Technique or Dry Cupping provides more beneficial effects than conventional treatment alone. 1\) Be divided into 2 Groups (Group A= Dry Cupping; B: Graston Techniques) 2) get the treatment for 4 weeks (3 days a week). 3) Receive the same conventional treatment.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-07-31; most recent amendment 2025-12-22.
Status change: Enrolling by Invitation → Completed 2025-11-27
Trial Details
NCT Number NCT07102355
Lead Sponsor University of Management and Technology Sialkot Pakistan
Conditions Scapulocostal Syndrome
Enrollment 46 participants
Start Date 2024-10-01
Primary Completion 2025-01-25 (estimated)
Study Completion 2025-09-13 (estimated)
Updated on ClinicalTrials.gov 2025-12-30