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Clinical Trials/NCT05625009
NCT05625009
Completed
Not Applicable

Comparison of Bilateral Ultrasound-Guided Transversus Abdominis Plane (Tap) Block and Erector Spinal Plane (Esp) Block in the Management of Postoperative Analgesia in Patients Who Had Cesarean Section Under Spinal Anesthesia

Istanbul Saglik Bilimleri University1 site in 1 country94 target enrollmentNovember 24, 2022
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ConditionsPain, PostoperativeCesarean SectionErector Spinae Plane BlockTransversus Abdominis Plane Block

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Postoperative
Sponsor
Istanbul Saglik Bilimleri University
Enrollment
94
Locations
1
Primary Endpoint
Percentage of patients needed for rescue analgesic agent (diclofenac)
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Transversus Abdominis Plane Block (TAPB) is frequently used for the management of postoperative pain in patients undergoing cesarean section. Recently, Erector Spinae Plane Block (ESPB) has been defined and used in several clinical scenarios. However, data regarding the ESPB use in the aforementioned patient group is limited.

Registry
clinicaltrials.gov
Start Date
November 24, 2022
End Date
April 2, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Istanbul Saglik Bilimleri University
Responsible Party
Principal Investigator
Principal Investigator

Taner Abdullah

Principal Investigator

Istanbul Saglik Bilimleri University

Eligibility Criteria

Inclusion Criteria

  • •18 - 45 years
  • •Undergoing cesarean section under spinal anesthesia

Exclusion Criteria

  • •History of chronic pain
  • •Body mass index \> 35
  • •Urgent/emergent surgeries
  • •Major bleeding
  • •Any additional surgical procedure
  • •Contraindication for any drugs used in the protocol
  • •The presence of any instrumentation in the procedure sites

Outcomes

Primary Outcomes

Percentage of patients needed for rescue analgesic agent (diclofenac)

Time Frame: 24 hours

Secondary Outcomes

  • Percentage of patients experienced chronic pain(2 months)
  • the dose of the opioid used(24 hours)
  • Percentage of patients needed for rescue analgesic agent (opioid)(24 hours)

Study Sites (1)

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