Recruitment

Recruitment Status
Not yet recruiting

Summary

Conditions
  • Amenorrhea
  • Major Depressive Disorder
Type
Interventional
Design
  • Allocation: N/A
  • Intervention Model: Single Group Assignment
  • Masking: None (Open Label)
  • Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 75 years
Gender
Both males and females

Description

The study will be up to 14 visits, which will occur for up to a 1 year period. The first visit is a screening visit, which will take about one hour to determine eligibility. If participants are eligible, participants will be scheduled for a baseline visit and 12 monthly visits to determine the antid...

The study will be up to 14 visits, which will occur for up to a 1 year period. The first visit is a screening visit, which will take about one hour to determine eligibility. If participants are eligible, participants will be scheduled for a baseline visit and 12 monthly visits to determine the antidepressant effects and possible side effects.

Tracking Information

NCT #
NCT04990687
Collaborators
Not Provided
Investigators
  • Principal Investigator: Jingping Zhao, MD Institute of Mental Health of The Second Xiangya Hospital, Central South University, 139# Renmin Middle Road?Changsha 410011, Hunan, P.R. China
  • Principal Investigator: Matthew Macaluso, M.D. The University of Alabama at Birmingham