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Comparison the effect of moxibustion & acupressure on severity of menstrual pain

Comparison the effect of moxibustion & acupressure at the point sp6 on severity of primary dysmenorrhea

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201505236807N17
Enrollment
100
Registered
2015-08-04
Start date
2015-02-14
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Primary dysmenorrhea. Primary dysmenorrhea

Interventions

Intervention 1: Intervention group1: in people with inclusion criteria To be attached moxa burning for 10 minutes,( twice with an interval of 48 hours, 4-5 days before their bleeding and 2 first day o
Treatment - Other
Intervention group1: in people with inclusion criteria To be attached moxa burning for 10 minutes,( twice with an interval of 48 hours, 4-5 days before their bleeding and 2 first day of bleeding) duri
Intervention group2: in people with inclusion criteria To be acupressure at sp6 points for 10 minute on each feet, ( twice with an interval of 48 hours, 4-5 days before their bleeding and 2 first day

Sponsors

The International Branch of Shahid Beheshti University of Medical Sciences& Health Services
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: being single; age between 18 – 25 year old; girls with primary dysmenorrhea that the pain intensity as moderate to severe based McGill ruler; do not suffering from chronic diseases (diabetes, hypertension, cardiac diseases, infectious diseases, liver, kidney); regular menstruation (period between 21 – 35 days); have not any symptoms of itching, abnormal discharge during study; not taking any medication, supplements; they should not use any herbal remedies about 3 months ago Intervention; they should not have any deplorable event such as near relatives’ death or surgical operation in recent six months; the absence of ulcer, varicose, cutaneous and inflammatory diseases at the point sp6. Exclusion criteria: individual's consent to continue participating in the study; pelvic known pathology(myoma, pelvic tumor, endometriosis, PID) during the study; improper use of moxibustion & acupressure; any use of herbal drug during the study; Sensitivity to moxa.

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Complications. Timepoint: Finally of bleeding days. Method of measurement: Questionnaire.

Primary

MeasureTime frame
Severity of primary dysmenorrhea. Timepoint: Before the intervention, while following intervention during the 3 first day of bleeding in 2 cycles. Method of measurement: Verbal Multidimensional Scoring System Questionnaire, McGill ruler.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSedigheh Amir Ali Akbari

Shaid Beheshti University of Medical Sciences

sedaliakbari@gmail.com+98 21 8820 2512

Outcome results

None listed

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