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The effect of wet-cupping on amenorrhea and oligomenorrhea

Evaluation the efficacy of calves wet cupping on vaginal bleeding induce in women with amenorrhea and oligomenorrhea.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016062728664N1
Enrollment
75
Registered
2016-08-04
Start date
2016-05-21
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

Condition 1: Pcos. Condition 2: Ovarian dysfunction. Polycystic ovarian syndrome Ovarian dysfunction, unspecified

Interventions

Calves wet-cupping will done at the 26th day of menstruation cycle. When the patient is in the prone position, calf muscle is suctioned repeatedly to provide a negative pressure. Then under aseptic co

Sponsors

Vice chancellor for research of Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 20-40 years old women with minimum 60 days menstruation retardation (from LMP); personal satisfaction; Not metformin or hormonal drugs users. Exclusion criteria: Use of hormonal or herbal drugs that affect menstruation; Positive BhcG; Lactation; Plannig to be pregnant during the next 3 months; History of thyroid dysfunction; History of anemia; History of coagulation diseases; History of diabetes mellitus; FSH >40; Hyperprolactinemia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Menstrual blood volume. Timepoint: Before intervention and 1, 2, 4 and 12 weeks after intervention. Method of measurement: Ask the patient and complete tracking form.;Occurance of Menstrual bleeding. Timepoint: Before intervention and 1, 2, 4 and 12 weeks after intervention. Method of measurement: Ask the patient.;Duration of menstural bleeding. Timepoint: Before intervention and 1, 2, 4 and 12 weeks after intervention. Method of measurement: Ask the patient and complete tracking form.

Secondary

MeasureTime frame
SHBG. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: SHBG serum assay.;Testosteron. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Serum testosteron assay.;Insulin resistance. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Fasting blood suger &insulin assay.;Quality of life. Timepoint: Before intervention and 4&12 weeks after intervention. Method of measurement: Ask the patient and complete tracking form.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzam Meyari

Traditional school of Shahid Beheshti University of Medical Sciences

d_a_meyari@yahoo.com; ameyari@sbmu.ac.ir+98 21 8877 3521

Outcome results

None listed

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