Expired Study
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Cleveland, Ohio 44106


Purpose:

Epidurally administered Depodur provides equal or superior analgesia as an epidural infusion of fentanyl for the first 48 hours after a cesarean section.


Criteria:

Inclusion Criteria: - Healthy pregnant women (ASA I or II) who are scheduled for an elective cesarean section - Patient appropriate for regional anesthesia - Patient agrees to receive regional anesthesia - Patient willing to have an epidural infusion of medication for two days postoperatively Exclusion Criteria: - Morbid obesity - History of sleep apnea - Allergy to opioids medications - History of opioids use during week prior to procedure - Emergency cesarean section - Significant surgical complications - Contraindication or refusal to have regional anesthesia - Age less than 18


NCT ID:

NCT00762554


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Cleveland, Ohio 44106
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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