Low Versus Standard Volume EXORA Block in Laparoscopic Cholecystectomy
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorFayoum University Hospital
About this trial
The original EXORA block used high local anesthetic volume (50 mL total), raising concerns about local anesthetic systemic toxicity (LAST). In such a bilaterally administered regional technique, evaluating the efficacy of a reduced-volume approach is warranted to maximize patient safety.
Eligibility criteria
Qualifiers
American Society of Anesthesiologists (ASA) physical status I or II.
Scheduled for elective laparoscopic cholecystectomy under general anesthesia.
Disqualifiers
• Patient refusal to participate.
Obese patients with a body mass index of more than 35 kg/m2.
Known cognitive impairment or use of psychiatric drugs
Known allergy to local anesthetics
Trial design
Treatments tested in this trial
- EXORA block 15
- EXORA block 25
Treatment groups
96 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov