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Comparison of the effect of Plantago Syrup and Mefenamic Acid Capsule Hypermernorrhea

Comparison of the effect of Plantago Syrup and Mefenamic Acid Capsule Hypermernorrhea

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017061634576N1
Enrollment
68
Registered
2017-08-19
Start date
2017-09-23
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

Hymenorrhea. Excessive and frequent menstruation with regular cycle

Interventions

Intervention 1: There are two intervention groups in the study group. The serum of Barragon syrup is given at 5 cc every 8 hours in the first 5 days of menstruation. In the other group, the muscle cap
Treatment - Drugs
Placebo
There are two intervention groups in the study group. The serum of Barragon syrup is given at 5 cc every 8 hours in the first 5 days of menstruation. In the other group, the muscle capsule is given ev
Placebo group Placebo syrup 5 cc every 8 hours with Mefenamic acid capsule is given one every 8 hours.

Sponsors

Deputy of Research and Technology of Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
36 Years to 45 Years

Inclusion criteria

Inclusion criteria: Criteria for entering the study of outpatients between the ages of 36-45 years with a complaint of hypernorrhoea that have negative pregnancy tests and not being breast-fed;The patient has no desire for hormonal treatment (ocp);Genic examination is normal;Pap smear sample of the patient is healthy;At the same time as hormonal treatments,Not use to other Herbal remedies and herbs; A month before entering in to the study,Doesn't use any drug to heal much hemorrhage;Use non-hormonal prevention;Hb is between 11 and 14;A patient with diabetes,Does not have uncontrolled blood pressure, congestive heart disease, and blood dislocations;The patient has no history of chronic diseases such as lupus and thyroid problems;The patient does not have a history of uterine malformations, ovaries, or other malignancies;Patient does not have hyperlichotheneemia ;Does not have IUD;The BMI is between 18/5 and 30;No fibroma.Exit criteria for patients who get pregnant during the study;Patients who use hormonal drugs during the study;Patients with possible side effects;Patients who require other interventions and have surgery;Patients who decide to leave the study with a personal request;The bleeding during the study is so severe that it requires emergency procedures.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity and duration of menstrual bleeding. Timepoint: Beginning of the study and after three periods. Method of measurement: PBAC chart.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMozhdeh Khodabakhsh

School of Traditional Medicine and Mashhad Supplement

khodabakhshm931@mums.ac.ir+98 51 3882 9279

Outcome results

None listed

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