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Therapeutic effect of moxibustion on primary dysmenorrhea: randomized clinical trials

Therapeutic effect of moxibustion on primary dysmenorrhea: randomized clinical trials

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000291
Enrollment
Unknown
Registered
2025-02-16
Start date
2023-10-13
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Primary dysmenorrhea

Interventions

Hot packs group:on demand
Moxibustion 2 group:Moxibustion at least three times a day for 15 to 20 min.
Moxibustion 1 group:Moxibustion at least once a day for 15 to 20 min.

Sponsors

Macau Polytechnic University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria (1) Voluntarily participate in this study and sign the informed consent form; (2) Normal mental consciousness able to communicate and socialize normally; those who have good compliance and can complete the experiment independently; (3) Women aged 18-30 years old with regular menstrual cycle and duration; (4) CMSS score >10; (5) A score of =4 on the Nagai pain scale.

Exclusion criteria

Exclusion criteria: Exclusion criteria (1) Those with severe organic pelvic and abdominal diseases (including those with and those who are not clearly known to have them); (2) Those with broken and damaged skin at the moxibustion site and those who are allergic to smoke heat or moxibustion.

Design outcomes

Primary

MeasureTime frame
Changhai pain scale;

Countries

China

Contacts

Public ContactSulan Sun

Macau Polytechnic University Macau SAR China

1779930223@qq.com17344054039

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026