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Effect of Sariva mool churna in Excessive Menstrual Bleeding

RANDOMISED CONTROLLED CLINICAL TRIAL TO EVALUATE THE EFFECT OF SARIVA MOOL CHURNA IN THE MANAGEMENT OF ASRUGDAR W.S.R. TO ABNORMAL UTERINE BLEEDING. - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112455
Enrollment
70
Registered
2026-06-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: N92- Excessive, frequent and irregularmenstruation

Interventions

None listed

Sponsors

DrSwapnali Mangesh Tathedeshmukh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient selected from age group 18 yrs to 50 yrs 2.Prolonged bleeding greater than 7 days 3.Quantitatively increase in menstrual bleeding .PBAC Score more than 100 4.Hb more than 7 gm /dl 5.Selection irrespective of marital status and parity

Exclusion criteria

Exclusion criteria: 1.Pregnant Women 2.Patient with post menopausal bleeding 3.Patient diagnosed with neoplasm 4.Patient with traumatic bleeding 5.Uterine and pelvic pathology like Fibroid(size more than 2 cm), polyp, Pelvic inflammatory disease,Tubo ovarian mass. 6.Any systemic disease like Diabetes mellitus, hypertension,Patient on anticoagulant therapy, HIV or VDRL or HbsAg positive patients. 7.Patient using any IUCD. 8.Patient with abortive bleeding. 9.Patient undergoing treatment for any other serious illness.

Design outcomes

Primary

MeasureTime frame
To evaluate the effect of sariva mool churna on amount of blood loss per vaginallyTimepoint: 3 month

Secondary

MeasureTime frame
To evaluate the effect of Sariva mool churna on Number of Per vaginal bleeding days. Associated symptoms like Angamard,Daurbalya,Bhrama.Timepoint: 3 month

Countries

India

Contacts

Public ContactDr Prashant Dalvi

M.A Podar Ayurvedic hospital,Mumbai

drdalvipn@gmail.com9822783636

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026