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Management of Indwelling Labor Epidural Catheters for Cesarean Delivery

NCT07366307 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2026-01-26

No results posted yet for this study

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.

Conditions

  • Intraoperative Pain

Sponsors & Collaborators

  • Baylor Research Institute

    lead OTHER

Principal Investigators

  • Michael P Hofkamp, M.D. · Baylor Scott & White Medical Center-Temple

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-01-01
Primary Completion
2026-12-31
Completion
2026-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07366307 on ClinicalTrials.gov