Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
FEMALE
ID06316583

Clinical Study of Dry Needling on Myofascial Trigger Points Treatment for Primary Dysmenorrhea and Preliminary Investigation of Its Relevance to Acupoints

Led by Beijing Hospital · Updated on 2025-05-21

150

Participants Needed

2

Research Sites

52 weeks

Total Duration

On this page

Sponsors

B

Beijing Hospital

Lead Sponsor

B

Beijing Municipal Health Commission

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Brief Title

Clinical Study on Dry Needling for Primary Dysmenorrhea and Its Preliminary Correlation With Acupoints

Who Can Participate

Age: 18Years - 30Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women diagnosed by a gynecologist with primary dysmenorrhea without pelvic organic lesions
  • Aged between 18 and 30 years
  • History of cyclical menstrual pain lasting more than 2 years
  • Pain greater than 30mm on the Visual Analog Scale (VAS, 0-100mm)
  • Willing to sign informed consent and cooperate with acupuncture treatment and study procedures
Not Eligible

You will not qualify if you...

  • Secondary dysmenorrhea or other reproductive and urinary system diseases such as endometriosis
  • History of pregnancy, miscarriage, or planning for pregnancy
  • Skin infections on the abdomen or lower back
  • Previous acupuncture or other needling treatments
  • History of mental illness or severe diseases of heart, liver, brain, kidneys, or blood system
  • Use of pain clinics, morphine, pethidine, or NSAIDs allergy within past 6 months
  • Current use of anticoagulant medications
  • History of adverse reactions to acupuncture such as fainting

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

Follow-up

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

Trial Site Locations

Total: 2 locations

1

Yanxia Sun

Beijing, Beijing Municipality, China, 100730

Actively Recruiting

2

Yanxia Sun

Beijing, Beijing Municipality, China, 100730

Actively Recruiting

Loading map...

Research Team

Y

Yanxia Sun

L

LiHua Yang

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

Similar Trials

Assessment Of Knee Joint Position Sense And Dynamic Balance ...

Primary Dysmenorrhea

Actively Recruiting

1 location

A Clinical Follow-up Study on the Efficacy of Thumbtack Need...

Postoperative Complications

Actively Recruiting

2 locations

A Study Assessing the Effects of Acupuncture in Parkinson's ...

Parkinson's Disease

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial

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/40933501