Management of Indwelling Labor Epidural Catheters for Cesarean Delivery

Management of Indwelling Labor Epidural Catheters and Pain During Cesarean Delivery: a Prospective Single-center Patient-reported Outcome Study

Status

Not yet recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT07366307

Enrollment

200

Registered

2026-01-26

Start date

2026-01-01

Completion date

2026-12-31

Last updated

2026-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intraoperative Pain

Keywords

cesarean section, pain, labor epidural catheter, top up

Brief summary

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 50 Years

Healthy volunteers

Yes

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

Design outcomes

Primary

Measure	Time frame	Description
Pain during cesarean delivery	Patients will be asked this question once 24-72 hours after their cesarean delivery.	Patients will answer "yes" or "no" to whether they experienced pain during their cesarean delivery.

Contacts

CONTACTMichael P Hofkamp, M.D.

Michael.Hofkamp@bswhealth.org254-724-3370

PRINCIPAL_INVESTIGATORMichael P Hofkamp, M.D.

Baylor Scott & White Medical Center-Temple

Outcome results