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Search / Trial NCT06320262

Evaluation of the Effect of Wet Cupping (Hijama) on Primary Fibromyalgia

Launched by RASMIA ELGOHARY · Mar 16, 2024

Trial Information

Current as of September 07, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying the effects of a treatment called wet cupping therapy combined with home-based exercise to see if it helps improve symptoms in women with primary fibromyalgia. Fibromyalgia is a long-term condition that causes widespread pain and can make everyday life challenging. The researchers want to find out if adding wet cupping to regular exercise can provide better relief from pain compared to just doing exercise alone.

To participate in this study, women aged 18 to 55 who have been diagnosed with primary fibromyalgia and experience moderate pain are eligible. Participants should not have used certain medications, like muscle relaxants or antidepressants, in the past year. If you join the study, you can expect to undergo wet cupping therapy alongside your exercise routine, and you'll be involved in a supportive environment that aims to help improve your quality of life.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • 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.
  • Exclusion Criteria:
  • Underlying rheumatic, malignant, metabolic, hematological, or neurological disorders.
  • Patients with bleeding disorders or receiving anticoagulants.
  • Previous use, within a year, or current use of skeletal muscle relaxants, antidepressants, antiepileptic drugs, corticosteroids, benzodiazepines, or tramadol
  • Patients with BMI ≤ 18 or ≥ 35.
  • Pregnant or lactating women.
  • Patients with severe anemia.

About Rasmia Elgohary

Rasmia Elgohary is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes through innovative trial design and rigorous scientific methodology. With a focus on ethical practices and regulatory compliance, Rasmia Elgohary collaborates with healthcare professionals, institutions, and stakeholders to facilitate robust clinical studies across various therapeutic areas. The organization prioritizes patient safety and data integrity, striving to contribute valuable insights that enhance therapeutic options and support the development of groundbreaking treatments.

Locations

Cairo, , Egypt

Patients applied

0 patients applied

Trial Officials

Mohamed Yousef, Professor

Principal Investigator

Kasr Alainy School of Medicine, Cairo University, Egypt

Maha M Sabr, Professor

Principal Investigator

National Research Center (NRC)

Dalia B Abdelbaky, A. Prof.

Study Chair

National Cancer Institute (NCI)

Dalia M Afifi, Consultant

Study Chair

Agouza Rheumatology and Rehabilitation, Armed Forces, Egypt

Gehad G Maghraby, Lecturer

Study Chair

Kasr Alainy School of Medicine, Cairo University, Egypt

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported