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Effect of herbal drug(Brinjasif) in the management of pre menstrual syndrome (PMS)

Effect of Brinjasif in management of premenstrual syndrome (PMS): A double-blind, randomized placebo-controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071615
Enrollment
40
Registered
2024-07-31
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: N943- Premenstrual tension syndrome

Interventions

Intervention1: Brinjasif: Brinjasif will be finely powdered and 2 capsules of 500mg TID will be administered orally for 13days 2 consecutive cycles (from 21st day of menstrual cycle to 3rd day of next

Sponsors

Luqman Unani Medical College Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Subject irrespective of their marital status, between 18-40 years having regular menstrual cycle of 21-35days. 2) Presenting with signs and symptoms of PMS for atleast 3 menstrual cycles as per ACOG guidelines.

Exclusion criteria

Exclusion criteria: Patients with 1) Irregular menstrual cycle. 2) Pregnancy, lactating and women on OCPs, HRT. 3) Diagnosed case of psychiatric disease. 4) Women with uncontrolled endocrine illness (DM, THYROID DISEASE, HTN).

Design outcomes

Primary

MeasureTime frame
Change in PMTS-O scale before and after the treatment.Timepoint: will be assessed at the baseline cycle during the treatment for the next consecutive treatment and after the treatment for one cycle

Secondary

MeasureTime frame
Change in VAS scale before & after the treatment.Timepoint: will be assessed at the baseline cycle during the treatment for the next consecutive treatment & after the treatment for one cycle

Countries

India

Contacts

Public ContactDr Nikhat Kausar Inamdar

Luqman Unani Medical College Hospital and Research Centre

nikhatinamdar72@gmail.com7019276469

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 27, 2026