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Effectiveness of Two Ayurvedic Medicines (Sunthi-Lodhara and Lajjalu Churna) in Treating Heavy Periods

Comparative clinical Trial to determine the effect of Shunthi-Lodhra Churna and Lajjalu Churna in management of Raktapradara w.s.r. to menorrhagia - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106162
Enrollment
80
Registered
2026-03-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

None listed

Sponsors

Dr Snehal Namdev Kakade
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients who will give informed written consent for study. 2 Patients of age group 18 to 49 years (reproductive age group). 3 The patients having clinical signs and symptoms of Raktapradara - Raja Ati Pravrutti (Excessive menstrual bleeding), Dirgha Kala Artava Pravrutti (Prolong menstrual bleeding more than 7 days), Vedana in Shroni Prushtha and Kukshi (Pain in the pelvic region), Yonigat Daha (Burning sensation in external genitalia), Daurbalya (Generalized Weakness), Angmard (Bodyache). 4 Hemoglobin percentage above 7 g/dl.

Exclusion criteria

Exclusion criteria: 1 K/C/O pelvic and uterine pathology like Uterine fibroid, Polyp, Pelvic inflammatory disease, Adenomyosis, Post-menopausal bleeding,malignant and non- malignant tumors. 2 K/C/O Any significant chronic illness. 3 K/C/O ectopic pregnancy, recent abortion, DUB. 4 K/C/O any external injury to reproductive track. Patients with IUCD and OCP pills. Patients taking Anti-coagulation therapy and having any coagulant defects like Thrombocytopenic Purpura.

Design outcomes

Primary

MeasureTime frame
Reduction in sign and symptoms of raktapradar such as raja aati pravrutti, Dirgha kala artava pravrutti, vedana in shroni, prushtha,kakshi,yonigat daha.Timepoint: Duration of study- 18 months Duration of treatment- 12 weeks Follow up - 2nd, 4th week of 3 consecutive menstrual cycles(12weeks).

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactDr Mangesh Moule

SST Ayurved mahavidyalay, Sangamner

mangeshmoule@gmail.com918485078771

Outcome results

None listed

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