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NCT07414407 · ClinicalTrials.gov registry record · NA
Impact of Patient Choice for Epidural Potency on Maternal Satisfaction
A NA study, sponsored by Stanford University.
- Not yet
- Registry status
- NA
- Development phase
- 150
- Enrollment target
NCT07414407: Clinical Trial NA study, sponsored by Stanford University.
NCT07414407 is a NA study that has not yet begun recruiting, run by Stanford University. The registered enrollment target is 150 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07414407, a NA study, has not yet begun recruiting, sponsored by Stanford University.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 150 participants
- Enrollment target
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.
Primary Outcome
Participant rating of overall satisfaction with pain care on a 5-point Likert scale (Describe your overall satisfaction with your epidural labor pain relief (Likert 1: very dissatisfied; 2: relatively dissatisfied; 3: fair; 4: relatively satisfied; 5: very satisfied)
Interventions
- PROCEDURE Patient-selected epidural management
- PROCEDURE Standard epidural management
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2026-04-01 |
| Est. Completion | 2030-12-31 |
| Phase | NA |
What is known before NCT07414407 opens enrollment
NCT07414407 is an interventional study that assigns participants to a tested intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower).
The record links to 0 conditions, and to 2 interventions - of which Patient-selected epidural management is the first listed.
NCT07414407 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT07414407 about?
NCT07414407 is a clinical study titled "Impact of Patient Choice for Epidural Potency on Maternal Satisfaction". 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 contro...
What is the current status of trial NCT07414407?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 150 participants. The study started on 2026-04-01. Estimated completion is 2030-12-31.
What interventions are being tested in trial NCT07414407?
The interventions under investigation include: Patient-selected epidural management (PROCEDURE), Standard epidural management (PROCEDURE).
Who is sponsoring clinical trial NCT07414407?
This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT07414407's enrollment target sits among peer trials
150 661st of 2000 higher than 1,299 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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