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To study the add on effectiveness of Palandu peya as a food in the management of Raktapradara(Menorrhagia)

A clinical study to evaluate the add on effectiveness of Palandu peya in Raktapradara(Menorrhagia).

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/01/022839
Enrollment
40
Registered
2020-01-17
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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: A Clinical study to evaluate the add on effectiveness of Palandu peya in raktapradara(menorrhagia): Shamana cikitsa with Bolabaddha rasa 2BD after food and Pushyanuga churna 5gm BD with

Sponsors

Dr Reshma Shaji
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects presenting with prolonged or excessive bleeding through vagina in normal cycles in at least past two cycles. Subjects in reproductive age group. Subjects ready to sign informed consent form.

Exclusion criteria

Exclusion criteria: Subjects with history of coagulation or fibrinolytic disease. Known case of sexually transmitted diseases. Subjects usually intrauterine devices and hormonal pills. History of malignancies. Diagnosed case of Inflammatory bowel disease.

Design outcomes

Primary

MeasureTime frame
A Clinical study to evaluate the add on effectiveness of Palandu peya as a pathya in the management of raktapradara(menorrhagia)Timepoint: Assessment will be done on baseline treatment,assessed on 15 th day and after completion of study on 31st day.

Secondary

MeasureTime frame
to reduce excessive bleeding and thereby preventing complications like anemia.Timepoint: 15 th day and after completion of study.

Countries

India

Contacts

Public ContactDr Reshma Shaji

Sri Manjunatheswara College of Ayurveda and Hospital

drmbkavita@sdmcahhassan.org9986432954

Outcome results

None listed

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