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A comparative clinical study to promote normal vaginal delivery without any complications to mether and fetus

A Randomized Comparative Clinical Study To Evaluate The Efficacy of two Different Ayurvedic Protocols on acheiving Sukhaprasava.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052700
Enrollment
60
Registered
2023-05-16
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: O759- Complication of labor and delivery, unspecified Health Condition 2: O80- Encounter for full-term uncomplicated delivery

Interventions

None listed

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient who are undergoing Garbhini Paricharya from 8th month of pregnancy in OPD AND IPD OF NIA Jaipur. 2.Pregnant women who completed 37 weeks of gestational age with sign of onset of labor and before 40 weeks with known LMP in Cephalic presentation with sign of onset of labor. 3.Pregnant woman of height more than 150cm . 4.Age between 21 to 35 years. 5.Hemoglobin 10 gm % or more

Exclusion criteria

Exclusion criteria: 1.Gravida having cephalo -pelvic disproportion ,Malpresentation ,Malposition ,history of antepartum haemorrhage , Bad obstetrics history , Multiple pregnancy , precious pregnancy or having any absolute indication for caesarean section . 2 .Gravida having systemic disease like diabetes mellitus ,tuberculosis, heart disease , chronic renal disease . 3 . Disease related to pregnancy like preeclampsia ,eclampsia ,polyhydramnios, oligohydramnios , Intra uterine growth restriction, Gestational diabetes ,Pregnancy indused hypertension , Premature rupture of membrane etc.. 4 .Previous ceaserian delivery within 5 year . 5 .Pregnancy with benign or malingnant tumors ,ovarian cyst ,uterine or cervical fibroid. 6. VDRL,HIV ,HBsAg positive pregnant woman

Design outcomes

Primary

MeasureTime frame
To achieve Sukhaprasava(Eutocia).Timepoint: 1day

Secondary

MeasureTime frame
Changes in the duration of 1st ,2nd ,and 3rd stages of labor.Timepoint: 1day

Countries

India

Contacts

Public ContactDr KBharathi

National Institute of Ayurveda

baruhunt@gmail.com9131207734

Outcome results

None listed

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