Clinical Trials Directory

Trials / Terminated

TerminatedNCT05711862

The Effects of Suvorexant on Sleep, Stress, and Cue-reactivity in Methamphetamine Use Disorder

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
7 (actual)
Sponsor
The University of Texas Health Science Center, Houston · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the effects of SUVO on sleep, stress, and cue reactivity/craving and to evaluate the preliminary safety and side effects profile of suvorexant (SUVO)

Conditions

Interventions

TypeNameDescription
DRUGsuvorexant (SUVO)Participants will receive 20mg of SUVO for 7 days. Participants will be directed to take the medication between 9:30 PM and 10:00PM.
DRUGPlaceboParticipants will receive 0mg of placebo for 7 days. Participants will be directed to take the medication between 9:30 PM and 10:00PM.

Timeline

Start date
2023-03-09
Primary completion
2024-03-28
Completion
2024-03-28
First posted
2023-02-03
Last updated
2025-04-29
Results posted
2025-04-29

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05711862. Inclusion in this directory is not an endorsement.

The Effects of Suvorexant on Sleep, Stress, and Cue-reactivity in Methamphetamine Use Disorder (NCT05711862) · Clinical Trials Directory