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Purslane effect on menorrhagia

The Comparison of the effect of Purslane and Mefenamic acid capsule on menorrhagia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201511263860N17
Enrollment
100
Registered
2016-04-19
Start date
2015-12-15
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

Menorrhagia. Excessive and frequent menstruation with regular cycle

Interventions

Intervention 1: Intervention Groups:Two mefenamic acid capsuls 250 mg every eight hours from first to third day of menstruation for two months and purslane capsule one hour after taking mefenamic aci
Treatment - Drugs
Intervention Groups:Two mefenamic acid capsuls 250 mg every eight hours from first to third day of menstruation for two months and purslane capsule one hour after taking mefenamic acid from first to
control Groups:Two mefenamic acid capsules 250 mg every eight hours from first to third day of menstruation for two months and placebo capsule one hour after taking mefenamic acid from first to third

Sponsors

Vice chancellor for research of School of Nursing and Midwifery of Shahid Beheshti University of Med
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria: being 18 to 40 years old; not having any pathologic problems and systematic diseases effective on hemorrhage like diabetes, coagulation disorders, hypo or hyperthyroidism, liver disorders or menstrual problems; not consuming any drugs effective on hemorrhage like aspirin, antidiabetics, antiepileptic, benzodiazepines, steroidal hormones or anticoagulants; not using hormonal contraceptive methods or IUDs; not having a history of abnormal pop smear or ultrasound (myoma, bicornuate uterus, endometrial hypertrophy, polyps, abnormal enlargement of the uterus); not being pregnant or intend to get pregnant during the next 3 months; not having diagnosed polycystic ovary syndrome; having a BMI withing the normal range

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The number of days of menstrual bleeding. Timepoint: Before intervention. The first menstrual cycle after the intervention. The second cycle of menstruation after intervention. Method of measurement: PBLAC Chart.;The volume of menstrual bleeding. Timepoint: Before intervention. The first menstrual cycle after the intervention. The second cycle of menstruation after intervention. Method of measurement: PBLAC Chart.

Secondary

MeasureTime frame
Side effects. Timepoint: The first menstrual cycle after intervention; second menstrual cycle after intervention. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGity Ozgoli

School of Nersing and Midwifery of Shahid Behesti University of Medical Sciences

g.ozgoli@gmail.com+98 21 8820 2512

Outcome results

None listed

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