Fibromyalgia Clinical Trials

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Evaluation of the Effect of Wet Cupping (Hijama) on Primary Fibromyalgia Using Brain Magnetic Resonance Spectroscopy and Patient-reported Forms: Randomized Controlled Clinical Trial

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Fibromyalgia has become one of the most prevalent chronic pain conditions that impair quality of life. Wet cupping has gained increasing popularity in treating painful conditions. This study aims to investigate the effectiveness of wet cupping therapy combined with home-based exercise compared to home-based exercise alone in improving patients diagnosed with primary fibromyalgia syndrome.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 55
Healthy Volunteers: f
View:

• Adult patients aged 18-55 years.

• Female individuals to avoid the gender confounding factor.

• Clinical diagnosis of primary fibromyalgia according to the 2016 American College of Rheumatology (ACR) updated diagnostic criteria.

• Moderate pain intensity of ≥ 45 mm or higher on a visual analog scale (VAS).

• No use of skeletal muscle relaxants, antidepressants, antiepileptic drugs, corticosteroids, benzodiazepines, and tramadol within a year before the screening visit.

Locations
Other Locations
Egypt
Rheumatology and Immunology out patient clinic, Internal Medicine Department, Cairo University
RECRUITING
Cairo
Contact Information
Primary
Rasmia M Elgohary, A. Prof.
rasmiaelgohary@kasralainy.edu.eg
01111370118
Time Frame
Start Date: 2024-12-26
Estimated Completion Date: 2025-12
Participants
Target number of participants: 50
Treatments
Active_comparator: Intervention group
They will receive wet cupping therapy (WCT) every month for 3 consecutive months in addition to a home-based graded exercise program.
No_intervention: Control group
they will receive a home-based graded exercise program, which is comprised of both aerobic and stretching exercises. The patients will be instructed to do the protocols with a gradual increase in both intensity and frequency.
Related Therapeutic Areas
Sponsors
Leads: Rasmia Elgohary

This content was sourced from clinicaltrials.gov