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To study the oral effect of jyotishmati vati in patient of aratavshaya

A RANDOMIZED OPEN LABELLED CONTROLLED CLINICAL TRIAL TO ASSESS AN EFFECT OF DURVA SWARASA BHAVIT JYOTISHMATI VATI IN ARTAVKSHAYA WITH SPECIAL REFERENCE TO OLIGOMENORRHEA

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/082543
Enrollment
90
Registered
2025-03-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: N915- Oligomenorrhea, unspecified

Interventions

None listed

Sponsors

Vd Manisha rajkumar vishwakarma
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 15 to 35 yrs. Selection irrespective of marital status, parity, socio-economic status. Patients having signs & symptoms of Artavkshaya. Those having scanty menstrual bleeding. Those females having quantity of bleeding less than 80 ml . Hb less than 8gm

Exclusion criteria

Exclusion criteria: Known patients of blood dyscrasias. Known patients of major systemic diseases that are likely to influence menstrual rhythm. For e.g.; HTN, DM, TB, HIV, Thyroid, Nephrotic disorders. Known patients of malignancy, cervical erosion, polyp, endometriosis, tubo-ovarian mass. Known case of structural anomalies of genital organs. Patients using IUCD’s. Patients undergoing treatment for any other serious illness.

Design outcomes

Primary

MeasureTime frame
To study the efficacy of durva swaras bhavit jyotishmati vati in artavkshaya with special reference to oligomenorrheaTimepoint: 3 months

Secondary

MeasureTime frame
To study detail about artavkshaya To study properties of durva swaras bhavit jyotishmati vatiTimepoint: 3 months

Countries

India

Contacts

Public ContactDr. Manisha Rajkumar Vishwakarma

Siddhakala ayurved mahavidyalaya and research centre sangamner

vipulbhujbal1@gmail.com9960840214

Outcome results

None listed

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