Oral Sedation in Vitreoretinal Surgery

Status Not yet recruiting

Clinical Trial Summary

The purpose of this study is to compare the efficacy of oral sedation to intravenous sedation with anesthesiology support and monitoring.

Clinical Trial Description

After being informed about the study and potential risks, and providing written informed consent, a total of 40 patients will undergo vitreoretinal surgery with oral Triazolam and 40 patients will undergo vitreoretinal surgery with intravenous sedation. The IV sedative will be determined by the anesthesiologist or certified registered nurse anesthetist but limited to midazolam, propofol, and fentanyl. The study will be a prospective, cross-sectional study with a 1:1 randomized procedure and unmasked. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04346095
Study type	Interventional
Source	Rocky Vista University, LLC
Contact
Status	Not yet recruiting
Phase	Phase 4
Start date	June 2020
Completion date	November 2020

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