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A Clinical study to evaluate the efficacy of tablet bramhi you with bruhat shatavari ghee and tablet manasamitra with bruhat shatavari ghee orally in the management of perimenopausal syndrome

An open label double arm randomised clinical study to evaluate the efficacy of bramhi vati with bruhat shatavari ghrita and manasamitra vati with bruhat shatavari ghrita orally in the management of perimenopausal syndrome - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090150
Enrollment
40
Registered
2025-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: N959- Unspecified menopausal and perimenopausal disorder

Interventions

None listed

Sponsors

Dr Pratiksha Mane
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects fulfilling diagnostic criteria. Subjects with age group of 40 – 55 years Subjects with symptoms of Perimenopausal Syndrome Both Married and Unmarried

Exclusion criteria

Exclusion criteria: Subjects who had undergone hysterectomy Subjects with history of systemic disorders which interfere with the course of treatment Women with psychological disorders

Design outcomes

Primary

MeasureTime frame
To evaluate and compare the efficacy of the bramhi Vati with bruhat shatavari ghrita and manasamitra vati with bruhat shatavari ghrita orally in the management of symptoms of perimenopausal syndromeTimepoint: One and half year—

Secondary

MeasureTime frame
NilTimepoint: Nil—

Countries

India

Contacts

Public ContactDr Anupama V

Sri kalbyaraveshwara swamy ayurvedic medical College hospital and research centre

dr.anupama.v@Gmail.com9845442660

Outcome results

None listed

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