Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
FEMALE
NCT06316583

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

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

150

Participants Needed

2

Research Sites

143 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 refers to menstrual pain not caused by pelvic organic lesions, commonly seen in young women, significantly affecting patients' quality of life. Dry needling therapy targeting myofascial trigger points for primary dysmenorrhea has been preliminarily applied in clinical settings. However, related research is limited with questionable quality, hindering its widespread clinical application. Furthermore, is there a connection between myofascial trigger points in dry needling and acupuncture acupoints in terms of selection and mechanism of action? Could this be a new interpretation of acupuncture theory? These are important questions that have garnered widespread attention. This study employs a randomized patient-blinded controlled design, enrolling primary dysmenorrhea patients aged 18 to 30 years. They are randomly divided into three groups: the trigger point dry needling group, traditional acupuncture treatment group, and trigger point sham needle (placebo) group. Changes in pain levels, quality of life scores, inflammatory factor levels, and local blood flow before and after treatment among the three groups are observed. The aim is to assess the therapeutic effects of dry needling trigger points and acupuncture treatments on primary dysmenorrhea and explore their potential mechanisms of action. By comparing the differences and similarities between dry needling trigger points and acupuncture treatments in terms of acupoint selection, treatment effects, and potential mechanisms of action, this study seeks to preliminarily explore the feasibility of integrating trigger point theory into the meridian 'acupoint' theory, laying the foundation for a modern interpretation of acupuncture

CONDITIONS

Official 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...

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

You will not qualify if you...

  • Having secondary dysmenorrhea or reproductive/urinary system diseases such as endometriosis
  • History of pregnancy, miscarriage, or planning pregnancy
  • Skin infections on the abdomen or lower back
  • Previous acupuncture or needling therapy
  • History of mental illness or severe heart, liver, brain, kidney, or blood system diseases
  • Used pain clinics, morphine, pethidine, or anticoagulants in the past 6 months
  • Allergic to NSAIDs or currently taking anticoagulant medications
  • Previous adverse reactions to acupuncture such as fainting

AI-Screening

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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

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Research Team

Y

Yanxia Sun

CONTACT

L

LiHua Yang

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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