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Completed NCT05886218

Quantitative Neuromuscular Monitoring and Gastric Bypass Surgery

Conditions: Sugammadex

Sex: All
Ages: 18 Years – N/A
Enrollment: 183
Sponsor: University of California, Davis

Location: UC Davis Medical Center Sacramento California

Summary

This is a single site, prospective, non-blinded, non-randomized, before/after study. This study is designed to evaluate the impact of monitoring and reversal guidelines for neuromuscular blocking drugs on the post-operative outcomes for patients undergoing laparoscopic gastric bypass surgery.

Eligibility Criteria

Inclusion Criteria: * age greater than 18 years * scheduled for an elective laparoscopic gastric bypass procedure Exclusion Criteria: * age less than 18 years * pregnancy * prisoners * significant co-existing lung disease including asthma or chronic obstructive pulmonary disease (COPD) requiring regular medication * patients who require supplemental oxygen pre-operatively to maintain a hemoglobin saturation (SpO2\>98%)

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05886218). StuddyBuddy aggregates publicly available trial information.