Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Opioid Use
  • Sedative Use
Type
Interventional
Phase
Phase 1
Design
Allocation: RandomizedIntervention Model: Crossover AssignmentMasking: Double (Participant, Investigator)Masking Description: This is a randomized, double-blind, double-dummy, placebo- controlled designPrimary Purpose: Basic Science

Participation Requirements

Age
Between 18 years and 55 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04315181
Collaborators
Not Provided
Investigators
Principal Investigator: Sharon L Walsh, Ph.D. University of Kentucky