Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
FEMALE
NCT07506044

Dexmedetomidine as an Adjuvant During Dural Puncture Epidural

Led by Menoufia University · Updated on 2026-04-01

140

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study aimed to determine the effects of using varied doses of DEX on the concentration of bupivacaine injected for epidural labor analgesia, and to assess the benefits of the dural puncture epidural.

CONDITIONS

Official Title

Dexmedetomidine as an Adjuvant During Dural Puncture Epidural

Who Can Participate

Age: 18Years - 40Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women in labor attending Emergency Department with cervical dilation of 3-5 cm
  • Normally positioned single fetus with intact fetal membranes
  • Free from exclusion criteria
Not Eligible

You will not qualify if you...

  • Abnormal fetal presentation or lie
  • Premature rupture of membranes
  • Maternal fever
  • Fetal distress
  • Pregnancy-induced diseases
  • Abnormal placental position
  • ASA grade higher than II
  • Marked obesity
  • Allergy or contraindications to study drugs
  • Spinal deformity or disorders
  • Skin diseases or infection at injection site

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Faculty of Medicine Menoufia University

Shebeen El Kom, Egypt, 32511

Actively Recruiting

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Research Team

R

Rabab Habeeb, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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