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A clinical trial to study effect of Yavani formulations on Menstrual Pain

Standard control clinical trial of various Kalpana of Yavani on Udavartini Yonivyapad with special reference to primary dysmenorrhoea

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/10/028604
Enrollment
200
Registered
2020-10-23
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Health Condition 1: N719- Inflammatory disease of uterus, unspecified

Interventions

Intervention1: Yavani Churna : Yavani. Botanical name : Trachyspermum ammi (Linn) Sprague. Family : Umbelliferae. A single blind comparative clinical study where minimum of 50 patients diagnosed as Ud

Sponsors

Dr Mauli Vaishnav
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients complaining painful menstruation at least two consecutive cycles. 2. Patient having regular menstrual cycle.

Exclusion criteria

Exclusion criteria: 1. Acute infection, 2. Acyclic and excessive bleeding more than 4 pads/day or more than 5days. 3. Any pelvic pathology leading to dysmenorrhoea 4. Intra Uterine Contraceptive Device induced painful bleeding 5. All secondary causes leading to dysmenorrhoea

Design outcomes

Primary

MeasureTime frame
Various kalpana of Yavani can be 70 % effective on Udavartini Yonivyapad WSR to Primary Dysmenorrhoea. Timepoint: After completion of 3 cycle of menstruation and 5 cycles of menstruation on the 4th day of menstrual cycle

Secondary

MeasureTime frame
Various kalpana of Yavani can provide 80 % beneficial effect on in pain during menstruation and provides beneficial effect on digestive system.Timepoint: on 3rd day of menstrual cycle

Countries

India

Contacts

Public ContactDr Mauli Vaishnav

Parul Institute of Ayurved, Parul University

rita.makim@paruluniversity.ac.in7990727524

Outcome results

None listed

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