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Evaluation of the Effectiveness of Kushmanda Khanda in Managing Menorrhagia (Asrigdara): A Clinical Study

A Clinical Study to evaluate the effect of Kushmanda Khanda in the management of Asrigdara. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073976
Enrollment
40
Registered
2024-09-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: N939- Abnormal uterine and vaginal bleeding, unspecified

Interventions

None listed

Sponsors

Narwade Pallavi Ashok
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients complaining of excessive bleeding more than 80ml and Increased duration of bleeding more than 7 days as a cardinal symptom.

Exclusion criteria

Exclusion criteria: Use of IUCD Patient with ongoing treatment of systemic disease like diabetes, hypertension. Uterine and pelvic pathology like polyps, fibroids, adenomyosis Endocrinal disease (Hypo/Hyperthyroidism) Non- Menstrual causes for bleeding (foreign body, genital malignancy, abortion, post-coital) Pregnancy Hb less than 9gm/dl PCOS Post – menopausal bleeding

Design outcomes

Primary

MeasureTime frame
Reduction in Bleeding Volume: Measure the average reduction in bleeding volume (ml) per episode after the intervention or treatment, aiming to bring the bleeding volume below 80 ml.Timepoint: 90 days

Secondary

MeasureTime frame
Duration of Bleeding: Measure the reduction in the duration of bleeding (hours or days) after the intervention, aiming to normalize the bleeding duration.Incidence of Excessive Bleeding: The proportion of participants who experience excessive bleeding (80 ml) after the intervention, compared to baseline.Hemoglobin Levels: Changes in hemoglobin levels before & after treatment, as excessive bleeding might lead to anemia.Quality of Life (QoL): Assess the impact of treatment on participants quality of life, including factors like pain, fatigue, & emotional well-being, possibly using a validated QoL questionnaire.Adverse Events: Incidence & severity of any adverse events related to the treatment or intervention used in the studyTimepoint: 90 days

Countries

India

Contacts

Public ContactNarwade Pallavi Ashok

Sri Jayendra Saraswathi Ayurveda College and Hospital, Chennai

drlrathnakar@sjsach.org.in9840340826

Outcome results

None listed

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