An open label double arm randomised controlled clinical study of Nonganadi ghrita orally on normal delivery

An Open Label Double Arm Randomised Controlled Clinical Study Of Nonganadi Ghrita on Prasava - NG

Status

Recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/070330

Enrollment

Registered

2024-07-09

Start date

Unknown

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery Health Condition 2: 1- Obstetrics

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Pregnant women willing for trial Patients fulfilling the criteria of full term(36 weeks) Age-21 to 35 years Primi gravida Cephalic presentation

Exclusion criteria

Exclusion criteria: Previous LSCS HIV, HBsAg, VDRL reactive subjects Absolute indication of cesarean section such as- central placenta previa, contracted pelvis or cephalo-pelvic disproportion, pelvic mass, advanced carcinoma cervix and vaginal obstruction. Any systemic disorders like hypertension, diabetes etc.

Design outcomes

Primary

Measure	Time frame
Favourable changes in the Bishops score Decrease in duration of three stages of laborTimepoint: 0day-30days	—

Secondary

Measure	Time frame
nilTimepoint: nil	—

Countries

India

Contacts

Public ContactDr Shweta Balamkar

SDM Institute of Ayurveda and Hospital, Anchepalya, Bangalore, Karnataka, 560074, India

Padmasarithareddy@gmail.com7353254151

Outcome results