Efficacy of Myofascial Trigger Point Dry Needling in Treatment of Primary Dysmenorrhea: A Study Protocol for a Three-Arm Randomized Controlled Trial.
Yanxia Sun, Lihua Yang, Lihong Zhu...
https://pubmed.ncbi.nlm.nih.gov/40933501Actively Recruiting
Led by Beijing Hospital · Updated on 2025-05-21
150
Participants Needed
2
Research Sites
52 weeks
Total Duration
B
Beijing Hospital
Lead Sponsor
B
Beijing Municipal Health Commission
Collaborating Sponsor
Primary dysmenorrhea is menstrual pain not caused by pelvic organic diseases, commonly affecting young women and greatly lowering their quality of life. This research evaluates dry needling therapy targeting myofascial trigger points and compares it with traditional acupuncture and placebo treatment. The study also explores the possible link between trigger points in dry needling and acupuncture points, aiming to provide a modern understanding of acupuncture theory. A randomized patient-blinded design enrolls women aged 18 to 30 with primary dysmenorrhea. Participants are randomly assigned to one of three groups: dry needling of trigger points, traditional acupuncture, and sham needling (placebo). Treatments occur once weekly for three weeks before menstruation. The dry needling group receives stimulation of specific muscle trigger points, while the acupuncture group receives needling at established acupoints. The placebo group receives sham needling without skin penetration. All participants perform abdominal stretching exercises 3 to 5 times daily for about 2 minutes each, continuing for one month. NSAIDs are allowed if pain becomes severe. During the study, researchers assess pain levels, quality of life, inflammatory markers, and local uterine blood flow before treatment, shortly after, and up to one year later. They also monitor medication use and adverse effects over an average of two years. Evaluations include pain scales, health surveys, and Doppler ultrasound to observe uterine circulation. This comprehensive approach aims to understand the treatment effects and mechanisms of dry needling and acupuncture for primary dysmenorrhea.
CONDITIONS
Clinical Study on Dry Needling for Primary Dysmenorrhea and Its Preliminary Correlation With Acupoints
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 3 weeks of treatment sessions plus 1 month of daily stretching exercises
Participants receive dry needling or acupuncture treatments once a week for three weeks before menstruation. They also perform abdominal stretching exercises 3 to 5 times daily for about 2 minutes each session for one month starting from the treatment day. Participants may take NSAIDs if they experience significant menstrual pain.
3 weekly visits (in-person) for treatment
Duration - Up to 1 year after treatment
Participants are observed for pain intensity, quality of life, inflammatory factors, and uterine blood flow up to one year after treatment completion.
Follow-up assessments at 1 month, 2 months, and 1 year after treatment
Total: 2 locations
1
Yanxia Sun
Beijing, Beijing Municipality, China, 100730
Actively Recruiting
2
Yanxia Sun
Beijing, Beijing Municipality, China, 100730
Actively Recruiting
Y
Yanxia Sun
L
LiHua Yang
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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Yanxia Sun, Lihua Yang, Lihong Zhu...
https://pubmed.ncbi.nlm.nih.gov/40933501