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Comparison of the immediate analgesic effect of perpendicular needling and transverse needling at SP6 in patients with primary dysmenorrhea

Comparison of the immediate analgesic effect of perpendicular needling and transverse needling at SP6 in patients with primary dysmenorrhea of cold and dampness stagnation syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026051
Enrollment
Unknown
Registered
2019-09-19
Start date
2019-09-30
Completion date
Unknown
Last updated
2019-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary dysmenorrhea

Interventions

Sponsors

Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Participants will be eligible if they are aged between 18 to 30 years old, have diagnosed as primary dysmenorrhea and have also diagnosed as cold-dampness stagnation pattern according to Traditional Chinese Medicine (TCM), the course of disease is 6 months to 15 years, have scores >= 40 mm on 100 on the VAS and no oral administration of any analgesic 24 hours before trial.

Exclusion criteria

Exclusion criteria: Patients with irregular menstruation, asthma, psychological diseases or life-threatening conditions (eg, disorders of the cardiovascular, liver, kidney or hematopoietic system) were excluded from this study. Patients with prior knowledge of acupuncture, those who had taken analgesic medication in the 24-hour period before the acupuncture intervention, and those who had potential problems with treatment compliance were also excluded.

Design outcomes

Primary

MeasureTime frame
VAS;

Secondary

MeasureTime frame
PI, RI, S/D in uterine arteries;BP, HR;Hamilton Anxiety Rating Scale;

Countries

China

Contacts

Public ContactMa Liangxiao

Beijing University of Chinese Medicine

maliangxiao@vip.sina.com+86 13301188102

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026