HEADING TOWARDS BETTERMENT OF PAINLESS DELIVERY OF PREGNANT WOMEN.

Not Applicable

Completed

• Registration Number: CTRI/2018/09/015751
• Lead Sponsor: A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2019-03-31
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 80

Inclusion Criteria

1.Parturients in established labour with cervical dilation >3cm, with intact or absent membranes and having satisfactory uterine contractions with >50% effacement.

2.Singleton pregnancy with vertex presentation at term,

3.Primigravidaor gravida 2 (previously normal delivered),

4.Age 18 years or above, weight less than 100kg, height 150 cm or more.

Exclusion Criteria

1.Patient refusal,

2.Any fetal anomalies,

3.History of coagulation disorders,

4.Any contraindications to epidural anaesthesia,

5.History of allergy to local anaesthetics,

6.Any obstetric complications (e.g., premature rupture of amniotic membranes,PIH),

7.Systemic and local sepsis,

8.Parturients having multiple pregnancies and premature labour,

9.History of peptic ulcer disease,

10.Known case of uncontrolled diabetes mellitus, and patient who had received dexamethasone in last 7 days for fetal lung maturity.

Study & Design

• Study Type: Interventional
• Study Design: Not specified