drugset / Trial / NCT06630390

Daridorexant to Prevent Delirium After Heart Surgery

NCT06630390

Phase 2 Completed 11 enrolled University of Rochester
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The goal of this phase 2 clinical trial is to demonstrate the feasibility of the current study methods and obtain preliminary data for an adequately powered trial of daridorexant with the aim of preventing delirium after heart surgery. The main aims this feasibility trial aims to answer are to demonstrate: (1) the feasibility of study recruitment; (2) the ability deliver study compounds to subjects according to the proposed methods; and (3) completeness of data capture; and (4) recording of potential adverse events. Participants will: (1) complete a baseline visit; (2) take the study drug--either daridorexant or placebo--each of the first 3 nights after heart surgery; and (3) be evaluated for sleep and delirium each of the first three days after heart surgery.

Timeline

Start
2024-11-11
Primary completion
2025-02-16
Completion
2025-02-16

Drugs

EvaluationDrugModalityDoseRoute
Subject Daridorexant Small molecule 50 mg Oral

Indications