Actively Recruiting
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
Eligibility Criteria
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
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
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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