About this trial
This is a prospective observational study that will survey patients who had an indwelling labor epidural catheter and subsequently underwent cesarean delivery. We hypothesize that patients who had removal of indwelling labor epidural catheters and had a new neuraxial anesthetic technique attempted will have a lower incidence of self-reported pain during cesarean delivery compared to patients who had top up of their indwelling labor epidural catheters.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
ages 18-50 years
had cesarean delivery at Baylor Scott & White Medical Center from January 1, 2026 through December 31, 2026
Fluent in the English language (our catastrophizing survey is validated in English language only)
Can provide their own consent
Disqualifiers
less than 18 years old, older than 50 years old
had cesarean delivery at Baylor Scott & White Medical Center before January 1, 2026 or after December 31, 2026
Employee of Baylor Scott & White Health labor and delivery unit
Student of a school that performs clinical rotations at Baylor Scott & White Medical Center-Temple
Trial population
Patients will be identified as potential study participants if they have a cesarean delivery at Baylor Scott \& White Medical Center-Temple from January 1, 2026 through December 31, 2025.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Pain during cesarean delivery
Patients will answer "yes" or "no" to whether they experienced pain during their cesarean delivery.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: