Impact of Patient Choice for Epidural Potency on Maternal Satisfaction

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-50
SponsorStanford University

About this trial

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.

Eligibility criteria

Qualifiers

Planned vaginal delivery

Patient requesting epidural labor analgesia

Gestational age >34 weeks

Disqualifiers

Any contraindication to neuraxial block

History of chronic pain, anxiety or depression

Intolerance or allergy to local anesthetic or opioids

Cesarean delivery within 2 hours of epidural initiation

Trial design

Treatments tested in this trial

  • Patient-selected epidural management
  • Standard epidural management

Treatment groups

150 Participants
are divided into 2 treatment groups

Sponsors and collaborators