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

Phase 2
Conditions
Health Condition 1: N943- Premenstrual tension syndrome
Registration Number
CTRI/2024/07/071615
Lead Sponsor
uqman Unani Medical College Hospital and Research Centre
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
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

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).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
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
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