Clinical Trials Directory

Trials / Completed

CompletedNCT03890406

The Effect of Deep Neuromuscular Blockade on Requirement of Intravenous Anesthetic Agent

The Effect of Deep Neuromuscular Blockade on Requirement of Intravenous Anesthetic Agent During Laparoscopic Colorectal Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
88 (actual)
Sponsor
Seoul National University Bundang Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Recently, deep neuromuscular blockade during general anesthesia has been studied by many authors regarding various effects upon patients' outcomes and surgical conditions. We believe deep neuromuscular blockade can be especially beneficial in laparoscopic surgery, because it can expand surgical space and prevent patients' minute movements that can disturb precise operations. In clinical situations, anesthetists tend to compensate the insufficiency of neuromuscular blockade by increasing the dose of other anesthetic agents, which can prolong patients' recovery time and impair the surgical condition. In this study, we plan to divide the patients into 2 groups according to the depth of neuromuscular blockade, and compare the dose of anesthetic agent used to maintain surgical condition.

Detailed description

Patients undergoing elective laparoscopic colorectal surgery are going to be recruited and divided into 2 groups: Group D will receive deep neuromuscular blockade, and Group M will receive moderate neuromuscular blockade using continuous infusion of rocuronium. Acceleromyography(TOF-watch SX) will be used to monitor the depth of blockade. In both groups, the anesthesia will be maintained with TIVA(total intra-venous anesthesia) including continuous target-controlled infusion of propofol and remifentanil. During the surgery, the number of patient movement and restoration of self respiration will be recorded. At the end of anesthesia, the dose of propofol and remifentanil used will be assessed and compared between the groups. Also, the satisfaction score of surgeons regarding the surgical condition, the anesthesia time, the operation time will be documented. After the patients are discharged, their charts are going to be reviewed and whether any pulmonary or surgical complications occurred will be documented.

Conditions

Interventions

TypeNameDescription
DRUGRocuronium: PTC(Post-tetanic count) 1~2Deep neuromuscular blockade will be maintained using continuous infusion of rocuronium.
DRUGRocuronium: TOF(Train-of-four) 1~2Moderate neuromuscular blockade will be maintained using continuous infusion of rocuronium.

Timeline

Start date
2019-04-01
Primary completion
2019-12-31
Completion
2020-03-31
First posted
2019-03-26
Last updated
2020-06-30

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03890406. Inclusion in this directory is not an endorsement.