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Efficacy and Mechanism of Yangyin Roujin Formula in Fibromyalgia Syndrome: A Randomized Controlled Trial

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

This prospective randomized, double-blind, controlled clinical trial is designed to address the current challenges in the clinical management of fibromyalgia (FM). We adopt Yangyin Roujin Formula, an empirical herbal prescription used in routine clinical practice, to evaluate its comprehensive therapeutic efficacy and safety in FM patients, including alleviating physical pain and common concomitant symptoms, improving physical function, and enhancing quality of life. Serum and fecal samples as well as brain MRI scans will be collected at baseline and after 12 weeks of intervention. The underlying mechanisms of this formula will be explored from multiple dimensions, including serology, gut microbiota-metabolome profiling, and central neuroimaging, so as to clarify the therapeutic advantages of Yangyin Roujin Formula for FM treatment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: t
View:

• Patients with primary fibromyalgia who met the FM classification criteria established by the American College of Rheumatology in 2016.

• TCM syndromes of liver qi stagnation and yin blood insufficiency, or hepatic and renal yin deficiency.

• aged 18 years old and above, 75 years old and below.

• pain VAS score ≥ 4.

• not taking the treatment of FM drugs or not using the treatment of FM program for more than 1 month.

• Sign the informed consent.

Locations
Other Locations
China
Guang'anmen Hospital of China Academy of Chinese Medical Sciences
RECRUITING
Beijing
Contact Information
Primary
Juan Jiao
jiao.juan@hotmail.com
010-88001132
Time Frame
Start Date: 2025-01-01
Estimated Completion Date: 2027-12-30
Participants
Target number of participants: 60
Treatments
Experimental: the YangyinRoujin Decoction group
Patients in the group received YangyinRoujin Decoction at a dose of 2 bags each time, twice daily for 12 weeks.
Placebo_comparator: the placebo group
The placebo was contained one-tenth of the dose of the original recipe. It was packaged in the same granule bag as the YangyinRoujin Decoction, ensuring that the placebo exhibited the same color, texture, taste, and smell as the actual medicine. Patients in the placebo group received placebo granule at a dose of 2 bags each time, twice daily for 12 weeks.
Related Therapeutic Areas
Sponsors
Leads: Juan Jiao

This content was sourced from clinicaltrials.gov