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Effect of a Unani drug in menopasual transitio

Not Applicable
Completed
Conditions
Health Condition 1: null- Menopausal transition symptoms
Registration Number
CTRI/2015/06/005868
Lead Sponsor
ational Institute of unani Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

•Menopausal transition women aged 35 or more

•Presence of any of these symptoms: menstrual changes, hypomenorrhoea, hot flushes, night sweats, sleep disturbances, palpitation, arthralgia, fatigue, anxiety, depression, urinary and sexual problems

•Women with early and late transition: Early transition: changes in cycle length of >=7 days either direction observed for at least two consecutive cycles or 60 days amenorrhoea. Late transition: 90 days to 11 months amenorrhoea.

Exclusion Criteria

•Women with known systemic and endocrine diseases like uncontrolled hypertension and diabetes mellitus, thyroid dysfunctions.

•Women with undiagnosed vaginal bleeding, history of surgical menopause.

•Women with hypersensitivity to drugs and past history of taken HRT within two months

•Pregnant and lactating women

•Women with any kind of malignancies

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The efficacy and safety of the test drug will be assessed by Menopausal Rating Scale (MRS).Timepoint: three months
Secondary Outcome Measures
NameTimeMethod
Improvement in menstrual irregularities (amenorrhoea, oligomenorrhoea and hypomenorrhoea)Timepoint: three months
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