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Study identifier: NCT05131178 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Post-operative Cesarean Trial of Pain Control

Condition: Post-operative Pain · Cesarean Section  ·  Sponsor: University of Colorado, Denver

PhaseNA
Planned participants100
Who can joinFemale, 18 Years to 50 Years
Healthy volunteersNo

About this study

This study plans to learn more about postoperative pain management after cesarean deliveries (C-sections). As a part of standard of care, the Children's Hospital Colorado's Colorado Fetal Care Center (CFCC) follows the standard Enhanced Recovery After Cesarean (ERAC) guidelines to manage pain following C-section delivery. In addition, the CFCC uses an FDA approved medical device called the ON-Q ® Pump, which continuously delivers local anesthetic medication to control pain in the area of your procedure. The local anesthetic used is bupivacaine, which is FDA approved for use to control local pain after C-sections. The CFCC has found a significant reduction in opioid use after adopting both of these procedures. The study aims to determine if the ERAC protocol or ON-Q ® Pump continuous infusion is responsible for lower opioid use by comparing bupivacaine (treatment) versus saline (placebo) groups.

This description comes directly from the study's public registry record.

Talk to the study team

Clinical Research Manager  ·  720-777-7080  ·  Kaylene.Ross@childrenscolorado.org

Deion Pena  ·  Deion.pena@childrenscolorado.org

Always discuss trial participation with your own doctor first.

Locations (1)

Children's Hospital ColoradoAurora, Colorado, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05131178