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A clinical study to evaluate the effect of Dadima churna in vomiting during early pregnancy.

An open Randomized controlled clinical study of Dadima churna in Garbhini chardi with special reference to emesis gravidarum in the first trimester of pregnancy - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102088
Enrollment
140
Registered
2026-01-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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 Komal Dattatry Wadje
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patient with confirmed intra uterine pregnancy having signs and symptoms of garbhini chardi . 2) Patient diagnosed as garbhini chardi i.e. morning sickness in first trimester. 3) Patient irrespective of parity, caste, income, group,occupation.

Exclusion criteria

Exclusion criteria: 1) Patient with Hyperemesis Gravidarum. 2) Patient in whom chardi seen in second and third trimester. 3) Vomiting caused due to other systemic disorders like acid peptic disorders, etc. 4) Gestational trophoblastic disease and multiple pregnancy.

Design outcomes

Primary

MeasureTime frame
To study the efficacy of Dadima churna 3gm with Koshna jala before meal twice a day against the standard control Doxylamine succinate 10mg and Pyridoxine hydrochloride 10mg before meal twice a day orally for 7 days in garbhini chardi w.s.r. to emesis gravidarum in the first trimester of pregnancyTimepoint: 7 days

Secondary

MeasureTime frame
1) To assess improvement by signs,symptoms(Nausea,frequency of vomiting,anorexia, weakness)and gradation of Assessment criteria. 2) To Achieve the control on Frequency of Vomiting of the patient. 3) To study etiopathology of Garbhini Chardi in detail according to Ayurveda & emesis gravidarum in detail according to modern text. 4) To achieve the outcome of study in 15 days.Timepoint: 7 days

Countries

India

Contacts

Public ContactDr Komal Dattatry Wadje

Yashwant Ayurvedic College post graduate training and Research centre kodoli

kvt126@gmail.com9423277612

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026