Ayurveda and Normal delivery

Phase 1

Completed

• Registration Number: CTRI/2018/03/012619
• Lead Sponsor: SIR SUNDER LAL HOSPITA

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2017-12-31
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 50

Inclusion Criteria

1. Pregnant women who willing for the trial and will give the written informed consent.

2.Both primigravida and multigravida of 34-35 weeks pregnancy with the age group between 20-30 years.

3.Pregnant women having gynaecoid or borderline pelvis ( normal pelvis measurement) with a normal lie and cephalic presentation.

Exclusion Criteria

1.Pregnant women who are not willing for trial.

2.Associated with any currently or going research study.

3.Age group <20 years and >30 years.

4.Pregnant women with Cephalopelvic disproportion(CPD), absolute contracted pelvis, malpresentation, multiple pregnancies, Cervical dystocia, History of Antepartum Haemorrhage, History of precipitate labour, history of absolute indication of caesarean section or (BOH), previous history of & recent history of Placenta Previa and having the macrosomic fetus in recent pregnancy.

5.Pregnant women having a systemic disease like Diabetes mellitus (DM), Hypertension (HTN), Tuberculosis (TB), Jaundice, heart disease, generalized oedema, severe anaemia, Renal diseases etc.

6.Pregnant women diagnosed with polyhydramnios, oligohydramnios, IUGR etc.

7.Benign and Malignant tumours and cysts of the genital tract.

8. Psychiatric patients.

9.Any allergy to the drug.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
cervical dilatation and effacement by Bishops Scoring, contraction frequency and duration, VRS AND VAS Scale scoring for pain during contractionTimepoint: at the time of admission in labour room and in active phase

Secondary Outcome Measures

Name	Time	Method
total duration of labour, duration of different stages of labour, Mode of delivery, PPH, cervical tear, Type of induction if requiredTimepoint: fron the latent stage of labour to the delivery of placenta