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Clinical Trials/TCTR20210813001
TCTR20210813001
Enrolling By Invitation
Phase 4

The comparison of efficacy between intrathecal morphine combined with either selective COX-II inhibitor or acetaminophen and intrathecal morphine alone for analgesia after cesarean section: a randomized control trial

/A0 sites88 target enrollmentAugust 13, 2021
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ConditionsOpioid consumption, quality of pain control, complication and satisfaction in postoperative period of elective cesarean sectionIntrathecal morphine, Acetaminophen, COX-II inhibitor, Non-steroidal anti-inflammatory drugs, NSAIDs, Cesarean section

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Opioid consumption, quality of pain control, complication and satisfaction in postoperative period of elective cesarean section
Sponsor
/A
Enrollment
88
Status
Enrolling By Invitation
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 13, 2021
End Date
October 22, 2021
Last Updated
last year
Study Type
Interventional
Sex
Female

Investigators

Sponsor
/A

Eligibility Criteria

Inclusion Criteria

  • •1\. Female participant age 18\-40 years old undergoing elective cesarean section
  • •3\. BMI 18\-40 kg/m2

Exclusion Criteria

  • •1\. Patient deny
  • •2\. Unable to communicate with researcher
  • •3\. Medication allergy or contraindication to medication which will be administered in this study
  • •4\. Contraindication of spinal anesthesia
  • •5\. Chronic opioid user

Outcomes

Primary Outcomes

Not specified

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