abour analgesia ( pain relief during labour)

Not Applicable

Completed

• Registration Number: CTRI/2019/04/018547
• Lead Sponsor: Institute of Medical Sciences Banaras Hindu University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2019-06-30
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

Patients belonging to ASA status 1 or 2

Above or equal to 38 weeks of pregnancy

Age group between 18-38 years

Hemodynamically stable

Pregnancy with no known feral malformation

Patients in labor pain having VAS score >3

Exclusion Criteria

Patients having allergies to opioids, amide group of local anaesthetic and non steroidal anti-inflammatory drugs

Patient refusal

Spinal deformity

Patients with deranged coagulation and bleeding parameters (INR >1.5)

Infection at puncture site of proposed epidural catheter

Presence of communicative or cognitive limitation interfering with pain measurement

Study & Design

• Study Type: Interventional
• Study Design: Not specified