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