Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
NCT06653036

Dural Puncture Epidural Vs Standard Epidural Technique in Parturient Receiving Continuous Labour Epidural Infusion

Led by Aga Khan University · Updated on 2025-01-30

38

Participants Needed

1

Research Sites

56 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this study is to evaluate the quality and safety of labor analgesia by comparing the use of Dural puncture epidural technique to Standard epidural technique while maintaining labor analgesia by means of continuous epidural infusion in parturient. The main questions it aims to answer are * Effectiveness and quality of labor analgesia * Frequency of catheter adjustments * Need for catheter replacements * Incidence of failed regional anesthesia requiring conversion to general anesthesia

CONDITIONS

Official Title

Dural Puncture Epidural Vs Standard Epidural Technique in Parturient Receiving Continuous Labour Epidural Infusion

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Nulliparous or multiparous women
  • Age over 18 years
  • ASA physical status 1 or 2
  • Singleton pregnancy with vertex (head-down) presentation
  • Gestational age between 37 and 42 weeks
  • Established labor with pain score of 3 or higher
Not Eligible

You will not qualify if you...

  • Major cardiac disease
  • History of chronic pain
  • Regular use of opioid medications
  • Platelet count less than 70 x 10^9/L
  • Spinal cord anomalies
  • Use of anticoagulant medications
  • Allergy to local anesthetics
  • Preeclampsia or eclampsia
  • Known fetal anomalies

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Aga Khan University

Karachi, Sindh, Pakistan

Actively Recruiting

Loading map...

Research Team

S

Samina Ismail, MBBS, FCPS

CONTACT

S

Sehrish Khan, MBBS, FCPS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here