Clinical Trials Directory

Trials / Terminated

TerminatedNCT00660062

Relapse Prevention With Escitalopram or Nortriptyline Following Electro-Convulsive Treatment (DUAG-7)

Relapse Prevention in Patients With a Major Depressive Episode Treated With Electroconvulsive Treatment Using a Fixed Dose Range of Escitalopram Compared to a Fixed Dose of Nortriptyline (DUAG-7) A Randomised Controlled 6 Month Double-blind Study

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
47 (actual)
Sponsor
Hillerod Hospital, Denmark · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The main purpose of this study is to investigate the relapse preventing efficacy of escitalopram in a dose range and nortriptylin in a single dose in patients having been treated successfully with a course of electroconvulsive treatment (ECT).

Detailed description

This study records severity of depression and relapse in patients treated for a major depressive disorder with electroconvulsive treatment (ECT)in a period og 6 month after end of ECT treatment. Patients will be randomized into four groups treated with escitalopram 10 mg, 20 mg, 30 mg or nortriptylin 100 mg daily dosages. The primary outcome measure is relapse and secondary outcome measure is tolerability. The study is a multicenter trial within Denmark.

Conditions

Interventions

TypeNameDescription
DRUGescitalopram10 mg daily
DRUGescitalopram20 mg daily dosage
DRUGescitalopram30 mg daily dosage
DRUGnortriptyline100 mg daily dosage

Timeline

Start date
2009-08-01
Primary completion
2014-11-01
Completion
2014-11-01
First posted
2008-04-17
Last updated
2014-12-09

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00660062. Inclusion in this directory is not an endorsement.