Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06553066

Deep Versus Moderate Neuromuscular Blockade in Bariatric Surgery

Deep Versus Moderate Neuromuscular Blockade in Bariatric Surgery:

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
University Hospital of Patras · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to investigate the effect of depth of neuromuscular blockade on the surgical field, patient postoperative pain, intestinal motility, the incidence of postoperative nausea and vomiting and the effect of deep versus moderate neuromuscular blockade on postoperative atelectasis quantitatively using chest computed tomography.This is a prospective, randomized, controlled clinical-controlled study in patients ≥18 years old scheduled to undergo elective bariatric surgery.

Conditions

Interventions

TypeNameDescription
DRUGDeep neuromascular blockagemaintenance of a deep neuromuscular block with rocuronium, titrated to maintain a TOF count of 0, and a PTC between 1-2. Quality of surgical field conditions' assessed by a blind surgeon as a 5 points scale(Leiden scale : 1 indicates extremely poor conditions, 2 poor conditions, 3 acceptable conditions, 4, good conditions and 5 optimal conditions)
DRUGModerate neuromascular blockagemaintenance of a moderate neuromuscular block with rocuronium, titrated to maintain a TOF count of 1-2

Timeline

Start date
2024-08-01
Primary completion
2026-08-01
Completion
2026-08-01
First posted
2024-08-14
Last updated
2024-08-14

Source: ClinicalTrials.gov record NCT06553066. Inclusion in this directory is not an endorsement.