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Effect of acupressure in dysmenorrhea

Comparison of acupressure effect of the third liver, fourth large intestine and placebo points on quality of life of girls with primary dysmenorrhea.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016052428038N1
Enrollment
90
Registered
2016-07-04
Start date
2015-04-21
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

Dysmenorrhea. Primary dysmenorrhoea

Interventions

LIV3 group: The LIV3 point (or third hepatic acupoint) is one of the hepatic meridians located at the point of bones junction. LI4 group: The LI4 point (HUGO) is located at the dorsal surface of the
Treatment - Other
LIV3 group: The LIV3 point (or third hepatic acupoint) is one of the hepatic meridians located at the point of bones junction. LI4 group: The LI4 point (HUGO) is located at the dorsal surface of the

Sponsors

Hormozgan University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 21 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: female gender; age between 18-21 years old; being single; regular menstrual period ( duration of 3-8 days and the interval of 21-35 days); a pain score of 4-10 according to the Wong-Baker faces pain scale; no genital disease; at least two hours passing after the last meal; absence of pain in all days of menstrual bleeding; no usage of oral or other contraceptives or drugs which disturb the ovulation cycle (NSAIDS, Analgesics, Prostaglandin synthesis inhibitors) four days before acupressure is started; lack of any abdominal/pelvic surgery; absence of tobacco consumption; not being alcohol consumer; absence of any speaking, visual, and auditory problems; absence of medical disease(cardio-vascular disease, nephropathy, respiratory disorders, diabetes, asthma, hypo/hyper thyroidism; absence of any severe psychological stress during the last six months(loss of relatives, etc); absence of any lesion, varices, or inflammatory skin disease at the location of applying pressure. Exclusion criteria: no desire of participant to cooperative in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain severity. Timepoint: Start of mensturation for two mentrural cycles. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Quality of life. Timepoint: start of mensturation for two mentrural cycles. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Fatemeh Bazarganipour

Hormozgan University of Medical Science

bazarganipour@hums.ac.ir; f.bazarganipour@gmail.com+98 76 3333 7192

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 9, 2026