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Effect of Bhrushtamudga Kashaya in Emesis Gravidarum

An open randomised Controlled clinical study to evaluate the efficacy of Bhrushtamudga Kashaya in Garbhini Chardi W S R to Emesis Gravidarum

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050965
Enrollment
90
Registered
2023-03-22
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Health Condition 1: O210- Mild hyperemesis gravidarum

Interventions

None listed

Sponsors

Dr Payal Ishwar Mandhalkar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient with intra uterine pregnancy having signs and symptoms of Garbhini Chardi . Patient diagnosed as Garbhini Chardi in first trimester. Patient irrespective of parity, caste,income group,occupation

Exclusion criteria

Exclusion criteria: Patient with Hyper Emesis Gravidarum. Patient in whom chardi seen in second and third trimester. Vomiting caused due to other systemic disorders like acid peptic disorders, etc. Gestational trophoblastic disease and multiple pregnancy.

Design outcomes

Primary

MeasureTime frame
To study the efficacy of Bhrushtamudga kashaya in Garbhini Chardi w.s.r. to Emesis Gravidarum on assessment of subjective parameters such as nausea frequency of vomiting anorexia weaknessTimepoint: 7 days

Secondary

MeasureTime frame
To reduce the signs and symptoms of Garbhini Chardi such as nausea frequency of vomiting anorexia weakness To assess improvement by signs symptoms and gradation of assessment criteria To study etiopathology of Garbhini Chardi in detail according to Ayurveda & Emesis Gravidarum in detail according to modern text To improve quality of life and reduce discomfort of the patient To achieve the outcome of study in 15 daysTimepoint: 15 days

Countries

India

Contacts

Public ContactDr Payal Ishwar Mandhalkar

Yashwant Ayurvedic College Kodoli

kvt126@gmail.com9423277612

Outcome results

None listed

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