Management of Indwelling Labor Epidural Catheters for Cesarean Delivery

Baylor Scott and White Health (BSWH)

Status: Not yet enrolling

Conditions: Intraoperative Pain

Study type: Observational

Funder types: Other

Identifiers

NCT07366307

025-604

Details and patient eligibility

About

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.

Enrollment: 200 estimated patients

Sex: Female

Ages: 18 to 50 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 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
• Identifies as Black or African American only, Hispanic, or White or Caucasian only
• had administration of local anesthetic through indwelling labor epidural or removal of indwelling labor epidural followed by single injection spinal or combined spinal epidural

Exclusion criteria

• 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
• Incarcerated at the time of study enrollment
• Underwent scheduled cesarean hysterectomy
• Underwent cesarean delivery with general anesthesia as either the primary anesthetic technique or had conversion to general anesthesia because of failure of neuraxial anesthesia
• Admitted to the intensive care unit immediately following cesarean delivery
• Did not have intrathecal morphine or intrathecal fentanyl if receiving spinal anesthesia
• Had anesthesia for an attempted external cephalic version within 24 hours of cesarean delivery

Trial design

200 participants in 1 patient group

Cesarean delivery patients

Description:

Patients who had an indwelling labor epidural catheter and subsequently underwent cesarean delivery.