Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Narcotic Use
  • Pain Postoperative
Type
Interventional
Phase
Phase 2
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Patients will receive either melatonin or a placebo for three nights prior to surgery and the investigator will measure pre-operative anxiety, preoperative sleep quality, post op pain medication consumption, post op pain scores, and blood values. The investigators would like to determine if melatonin can prevent preoperative anxiety, improve preoperative sleep, prevent excess narcotic consumption, and decrease post operative inflammation.Masking: Double (Participant, Care Provider)Masking Description: The surgeon and the patient will be masked, the research coordinator will not be masked.Primary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 35 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04791943
Collaborators
Not Provided
Investigators
Principal Investigator: Jason Baker, DMD Montefiore Medical Center