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NCT05625009 Clinical Trial

Bilateral Ultrasound-Guided Transversus Abdominis Plane (Tap) Block and Erector Spinal Plane (Esp) Block

Pain, Postoperative Clinical Trial

Official title:
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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05625009
Other study ID # 2021.10.227
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 24, 2022
Est. completion date April 2, 2023

Study information
Verified date May 2023
Source Istanbul Saglik Bilimleri University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 94
Est. completion date April 2, 2023
Est. primary completion date January 24, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - 18 - 45 years - ASA2 - 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

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Procedure/Surgery: Transversus Abdominis Plane Block (TAPB)
Patients received TAPB postoperatively
• Procedure/Surgery: Erector Spinae Plane Block (ESPB)
Patients received ESPB postoperatively

Locations
Country Name City State
Turkey Istanbul Basaksehir Cam and Sakura City Hospital Istanbul

Sponsors (1)
Lead Sponsor Collaborator
Istanbul Saglik Bilimleri University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Percentage of patients needed for rescue analgesic agent (diclofenac) 24 hours
Secondary Percentage of patients needed for rescue analgesic agent (opioid) 24 hours
Secondary the dose of the opioid used 24 hours
Secondary Percentage of patients experienced chronic pain 2 months
See also
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