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Effects of Injection Volume and Site on Sensory Distribution After Rectus Sheath Block

Study acronym: RSB-SENSE
StatusNot Yet Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Minor Study First Submitted
This randomized controlled study aims to evaluate the effects of local anesthetic injection volume and injection site on cutaneous sensory distribution following ultrasound-guided rectus sheath block (RSB). Participants undergoing laparoscopic abdominal surgery will be randomized to receive RSB using different injection sites and volumes (20 mL or 30 mL per side). Injection sites will be selected according to the surgical location, including upper, middle, or lower rectus sheath approaches. Cutaneous sensory distribution will be assessed to determine the extent and pattern of sensory blockade associated with each technique. The findings may help optimize injection techniques and local anesthetic volumes to achieve adequate sensory coverage for abdominal surgery.
Trial Details
NCT Number NCT07876297
Lead Sponsor Chiang Mai University
Conditions
(from sponsor)
Cutaneous Sensory Blockade
Related terms Agnosia
Enrollment 120 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov