NCT06274307

Efficacy of Transversus Abdominis Plane Block

Efficacy of Transversus Abdominis Plane Block in an Insufflated Abdomen
Justin Hruska·ClinicalTrials.gov·procedureRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Anesthesia, Local
Drug/Device/Intervention
Transversus abdominis plane block
Study type
Interventional
Intervention type
procedure
Sponsor & location
Primary sponsor
Justin Hruska
Funder
Wayne State University
Location
Detroit,Detroit, United States of America
Timeline & enrollment
Phase
N/A
Start date
Jun 22, 2023
End date
Sep 01, 2024
Enrollment
120 participants
Primary outcome

Time to perform TAP Block,TAP block attempts,Pain Score Visual Analog Scale (VAS) 0 Hours Post Surgery,Pain Score Visual Analog Scale (VAS) 1 Hours Post Surgery,Pain Score Visual Analog Scale (VAS) 2 Hours Post Surgery,Pain Score Visual Analog Scale (VAS) 4 Hours Post Surgery,Pain Score Visual Analog Scale (VAS) 24 Hours Post Surgery,Postoperative Opioid Consumption,Ease of performing TAP Block-anatomical plane visualization,Ease of performing TAP Block-performance efficacy,Patient satisfaction

Summary

This study aims to assess the efficacy of Transversus Abdominus Plane (TAP) blocks, a
 well-established anesthetic technique, to decrease the amount of post-operative pain in
 patients who undergo minimally invasive gynecologic surgeries. During minimally invasive
 gynecologic surgeries, the abdomen is inflated with pressurized air for visualization
 purposes and released at the end of the surgery. Traditionally, TAP blocks are performed by
 injecting long-acting local anesthetic agents under ultrasound guidance into the abdominal
 wall after abdominal surgery after the air has been emptied from the abdomen for additional
 anesthetic coverage post-operatively. This study proposes a novel approach: that performing
 TAP blocks while the abdomen is still insufflated will result in better post-operative pain
 outcomes as compared to the traditional method.

ICD-10 classifications
Local anaestheticsAnaesthetic, unspecifiedOther and unspecified general anaestheticsPoisoning: Local anaestheticsParenteral anaesthetics
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06274307
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06274307 through Pure Global AI's free database. This phase not specified trial is sponsored by Justin Hruska and is currently Recruiting. The study focuses on Anesthesia, Local. Target enrollment is 120 participants.

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