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Neuroaxial Labour Analgesia

NCT03980951 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2020-03-24

No results posted yet for this study

Summary

The primary outcome of this clinical trial is to compare the pain scores during labour and delivery of combined spinal epidural without intrathecal opioids and dural puncture epidural

The secondary objective of this study is to compare the and fetomaternal outcomes

Conditions

  • Labor Analgesia

Interventions

PROCEDURE

Dural Puncture Epidural Technique

three labor analgesia techniques

PROCEDURE

Combined Spinal Epidural without intrathecal opioids

three labor analgesia techniques

PROCEDURE

epidural

three labor analgesia techniques

Sponsors & Collaborators

  • elite medical hospital

    collaborator UNKNOWN

  • Wahba bakhet

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-12-01
Primary Completion
2018-05-01
Completion
2019-06-01

Countries

  • Egypt
  • Kuwait

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03980951 on ClinicalTrials.gov