Suicide Prevention by Lithium - the Lithium Intervention Study

NCT00520026 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 167

Last updated 2007-08-23

No results posted yet for this study

Summary

The purpose of this study is to examine the proposed suicide preventive effects of lithium in a randomized controlled trial within a group of individuals with depressive disorders. The hypothesis being tested is that lithium treatment will significantly reduce the risk for another suicide attempt.

Conditions

  • Suicide
  • Depressive Disorders

Interventions

DRUG

lithium

DRUG

placebo

Sponsors & Collaborators

  • German Federal Ministry of Education and Research

    collaborator OTHER_GOV
  • Sanofi

    collaborator INDUSTRY
  • Technische Universität Dresden

    collaborator OTHER
  • University of Bonn

    collaborator OTHER
  • Charite University, Berlin, Germany

    collaborator OTHER
  • University of Erlangen-Nürnberg

    collaborator OTHER
  • University Hospital Schleswig-Holstein

    lead OTHER

Principal Investigators

  • Fritz Hohagen, Prof. · Department of Psychiatry and Psychotherapy, Universitätsklinikum Schleswig-Holstein, Campus Luebeck

  • Bruno Müller-Oerlinghausen, Prof. · Former Research Group Clinical Psychopharmacology, Department of Psychiatry and Psychotherapy, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin

  • Werner Felber, Prof. · Department of Psychiatry and Psychotherapy, Medizinische Fakultät der Technischen Universität Dresden

  • Bernd Ahrens, PD · Department of Psychiatry and Psychotherapy, Universitätsklinikum Schleswig-Holstein, Campus Luebeck

  • Erik Lauterbach, Dr. · Department of Psychiatry and Psychotherapy, Universitätsklinikum Schleswig-Holstein, Campus Luebeck

  • Thomas Bronisch, Prof. · Max-Planck-Institute of Psychiatry Munich

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-01-31
Completion
2006-06-30

Countries

  • Germany

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00520026 on ClinicalTrials.gov