Clinical Trials Directory

Trials / Completed

CompletedNCT00295347

Mineralocorticoid Receptor in the Treatment of Severe Depression

Mineralocorticoid Receptor in the Treatment of Severe Depression: A Randomized, Double Blind, and Placebo Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
65 (estimated)
Sponsor
Universitätsklinikum Hamburg-Eppendorf · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The proposed research aims to compare the onset of action and the efficacy of fludrocortisone, a mineralocorticoid receptor agonist vs. spironolactone, a mineralocorticoid antagonist, vs. placebo as augmentation to a selective serotonin reuptake inhibitor (SSRI) in 65 inpatients with severe depression. The study will also explore the utility of the hypothalamic-pituitary-adrenal (HPA) axis in predicting treatment response. The study will be a 5-week randomized and double-blind trial of fludrocortisone vs. spironolactone vs. placebo during three years.

Conditions

Interventions

TypeNameDescription
DRUGSpironolactone
DRUGfludrocortisone
DRUGescitalopram

Timeline

Start date
2005-12-01
Primary completion
2008-06-01
Completion
2008-06-01
First posted
2006-02-23
Last updated
2017-05-30

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00295347. Inclusion in this directory is not an endorsement.