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VIJYADI VATI AND KUBERAKSHA VATI IN KRICCHARTAVA (DYSMENORRHOEA)

A Comparative Clinical Study of Vijayadi Vati and Kuberaksha Vati in the Management of Kashtartava With Special Reference to Primary Dysmenorrhoea.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/11/010472
Enrollment
100
Registered
2017-11-13
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: null- chief complaint of dysmenorrhoea with scanty or average amount of menses, along with or without associated symptoms and dysmenorrhoea since more than 2 consecutive cycles.

Interventions

Intervention1: Vijayadi Vati: Group A: Minimum 50 patients of Kashatartava will be treated by Vijayadi Vati orally. Dose - 500mg twice a day with lukewarm water. Duration - Drug will be started 5 days

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient coming with chief complaint of dysmenorrhoea with scanty or average amount of menses. 2. Patient in age group of 16 to 30 years. 3. Patient having H/O dysmenorrhoea along with or without associated symptoms. 4. Patient suffering from dysmenorrhoea since more than 2 consecutive cycles.

Exclusion criteria

Exclusion criteria: 1. Patient having any organic pathology of uterus and adnexae. 2. HIV, VDRL, HBsAg positive patient. 3. Patient suffering from systemic diseases. 4. Patient with Intra uterine contraceptive devices. 5. Patient with menorrhagia and metrorrhagia. 6. Patient having menstrual period interval less than 21 days or more than 35 days.

Design outcomes

Primary

MeasureTime frame
Pain assessment on Visual Analog Scale Numeric Rating ScaleTimepoint: 1. First follow up is done during trial after Second menses. 2.Final outcome is assessed after completion of trial in the next consecutive menses.

Secondary

MeasureTime frame
nausea, vomiting, giddiness, constipation, breast tenderness, diarrhea, headache, faintingTimepoint: 1. First follow up is done during trial after Second menses. 2.Final outcome is assessed after completion of trial in the next consecutive menses.

Countries

India

Contacts

Public ContactDr Priyanka Sharma

National Institute of Ayurveda

ps.17julyacad@gmail.com8988005960

Outcome results

None listed

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