Status:
NOT_YET_RECRUITING
Deep Versus Moderate Neuromuscular Blockade in Bariatric Surgery
Lead Sponsor:
University Hospital of Patras
Conditions:
Neuromuscular Blockade
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief 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 ...
Eligibility Criteria
Inclusion
- Patients aged ≥18 years ASA II-III who are to undergo planned laparoscopic bariatric surgery
Exclusion
- ASA 4 patients
- Maternal population
- Patients who are not scheduled to receive general anesthesia, but some other type of anesthesia.
- Contraindicated patients: administration of neuromuscular blockade, suppression of spontaneous respiration, and those with an indication for awake intubation or surgical airway.
- Patients with neuromuscular diseases
- Patients who refuse to participate in the study.
Key Trial Info
Start Date :
August 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 1 2026
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT06553066
Start Date
August 1 2024
End Date
August 1 2026
Last Update
August 14 2024
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