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Comparing Intrathecal Morphine and Erector Spinae Plane Regional Anesthesia Against Intrathecal Morphine Alone for Post-Cesarean Section Pain
The objective of the study is to optimize post-operative analgesia and improve patient satisfaction while reducing total opioid consumption after cesarean section
Age
18 - 45 years
Sex
FEMALE
Healthy Volunteers
No
Start Date
July 10, 2024
Primary Completion Date
September 10, 2024
Completion Date
September 10, 2024
Last Updated
September 19, 2024
erector spinae plane block (ESP)
PROCEDURE
Duramorph
DRUG
Ropivacaine
DRUG
Bupivacaine Injection
DRUG
Lead Sponsor
University of Miami
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06269770