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A study for moxibustion robot in treatment of primary dysmenorrhea patients with qi stagnation and blood stasis

A study for moxibustion robot in treatment of primary dysmenorrhea patients with qi stagnation and blood stasis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018236
Enrollment
Unknown
Registered
2018-09-06
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-09-10

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

Conditions

primary dysmenorrhea

Interventions

Group 1:Moxibustion robot moxibustion treatment
Group 2:Manual moxibustion treatment

Sponsors

Traditional Chinese Medicine Hospital of Sichuan
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Conformance to the diagnostic criteria of Chinese and Western medicine and signing an informed consent in writing; 2. aged between 18 and 35 years old; 3. In the acute episode of dysmenorrhea, visual analogue scale (VAS) for abdominal pain is more than 40 painkillers; 4. not taking acesodyne medication within the last 3 months. Patients in accordance with all of the six items mentioned above can be included in our study.

Exclusion criteria

Exclusion criteria: 1. having suffered from serious cardiovascular, digestive, renal, respiratory, hematological, neurological, endocrinological diseases, and so forth; 2. having suffered from spontaneous bleeding tendency ; 3. being participating in other clinical trials. Patients in accordance with any of the 8 itesm mentioned above will be excluded.

Design outcomes

Primary

MeasureTime frame
Pain Rating Index;Degree of angina pectoris (VAS score);pain rating index;the Cox Menstrual Symptom Scale;grading table of qi stagnation and blood stasis syndrome;the MOS item short from health survey;

Countries

China

Contacts

Public ContactTU Haiyan

Sichuan University

haiyantu@163.com+86 13881815191

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 23, 2026