Clinical Trial

Impact of Patient Choice for Epidural Potency on Maternal Satisfaction

Not Yet Recruiting
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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.
Trial Details
NCT Number NCT07414407
Lead Sponsor Stanford University
Conditions Epidural Analgesia, Obstetric, Maternal Satisfaction
Enrollment 150 participants
Start Date 2026-04-01
Primary Completion 2030-12-31 (estimated)
Study Completion 2030-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-02-17