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Impact of Patient Choice for Epidural Potency on Maternal Satisfaction

NCT07414407 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2026-02-17

No results posted yet for this study

Summary

This clinical trial will compare two different approaches to epidural analgesia during labor to see which approach leads to higher patient satisfaction after delivery.

Primary aim: determine whether one approach produces greater postpartum maternal satisfaction.

Secondary aims: compare pain control and side effects.

Participants are people in labor who receive epidural analgesia. They will receive routine clinical epidural care and complete brief, in-hospital questionnaires about pain and satisfaction.

All care is provided by the clinical team and safety practices remain unchanged.

Conditions

  • Epidural Analgesia, Obstetric
  • Maternal Satisfaction

Interventions

PROCEDURE

Patient-selected epidural management

Choice of epidural regimen

PROCEDURE

Standard epidural management

Hospital's usual epidural regimen

Sponsors & Collaborators

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2026-04-01
Primary Completion
2030-12-31
Completion
2030-12-31

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT07414407 on ClinicalTrials.gov