Clinical Trials Directory

Trials / Completed

CompletedNCT05822817

Comparison of Postoperative Recovery of Sevoflurane and Propofol After Transsphenoidal Surgery

A Prospective, Randomized Controlled Study to Compare the Effect of Sevoflurane and Propofol for Maintenance of Anesthesia on Postoperative Recovery After Transsphenoidal Resection of Pituitary Adenoma

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
252 (actual)
Sponsor
Peking Union Medical College Hospital · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Currently, total intravenous anesthesia (TIVA) and inhaled anesthesia are both commonly used for transsphenoidal pituitary adenoma resection. However, optimal choice for anesthesia maintenance in transsphenoidal surgery remains unclear. Previous studies focusing on this question provided fragmentary assessment and controversial results. The goal of this clinical trial is to investigate whether propofol and sevoflurane have different effect on post-anesthetic recovery after transsphenoidal resection of pituitary adenoma.

Conditions

Interventions

TypeNameDescription
DRUGsevofluraneAnesthesia is maintained with inhalation of sevoflurane. The concentration of sevoflurane was adjusted to maintain anesthetic depth, aiming for a bispectral index of 40-60.
DRUGpropofolAnesthesia is maintained with an effect-site target-controlled infusion of propofol (2-6ug/ml) based on the Marsh mode. The concentration of propofol was adjusted to maintain anesthetic depth, aiming for a bispectral index of 40-60.

Timeline

Start date
2023-05-03
Primary completion
2024-04-29
Completion
2024-08-14
First posted
2023-04-21
Last updated
2025-06-08

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05822817. Inclusion in this directory is not an endorsement.