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A clinical study of Unani Drug on Menorrhagia

A CLINICAL EVALUATION OF UNANI FORMULATION IN THE MANAGEMENT OF KASRAT-E-TAMS (MENORRHAGIA)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/08/045012
Enrollment
40
Registered
2022-08-29
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: N920- Excessive and frequent menstruation with regular cycle

Interventions

Intervention1: Tranexemic acid: 500mg tds orally from 3rd day of cycle for 15 days in tablet form for 3 cycles Control Intervention1: Extract of Unani Polyherbal Formulation- Anjbar(� Poligonum bis

Sponsors

Ayurvedic and Unani Tibbia College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women in the age group of 20 to 40 years. Women who have more than 80 ml blood loss during their menstrual cycle. Patients willing to sign the informed consent follow the protocol and participate in clinical trial voluntarily. The patient with PCOD, Ovarian cyst.

Exclusion criteria

Exclusion criteria: The patient with uterine fibroid. The patient was unwilling to sign the consent form. The patient has a history of AIDS, syphilis, and gonorrhoea. History of cardiovascular, renal, or liver disease History of diabetes (Type 1 or Type 2) Patients with systemic disease and malignancy Individuals of alcohol and other substance abuse. Pregnant and lactating women. Females who become pregnant during the study become excluded. Individuals who have a history of drug therapy used three months previous to enrolment in the study. Individuals with untreated thyroid disease/bleeding disorders. Patient having IUCD.

Design outcomes

Primary

MeasureTime frame
� To assess the safety of Unani formulations in the management of Kasrat-etams(menorrhagia). � To assess the efficacy of Unani formulations in the management of Kasrat-e tams(menorrhagia)Timepoint: 3 months

Secondary

MeasureTime frame
To evaluate the improvement of quality of life in test group patients Timepoint: 3 months

Countries

India

Contacts

Public ContactDr Varda Naaz

Ayurvedic and Unani Tibbia College and Hospital

draysharaza11@gmail.com9354925031

Outcome results

None listed

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