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Evaluation of Sub-syndromal Symptoms After Acute Depressive Episode in Bipolar Disorder

NCT01663974 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 125

Last updated 2015-03-09

No results posted yet for this study

Summary

The study aims to evaluate:

* the frequency of subsyndromal symptoms or disorders observed during interepisode phases in bipolar patients, particularly after a depressive episode in which these subsyndromal disorders are the most frequent
* the functional impact of these disorders, factors or symptom thresholds associated with functional remission, and factors associated with symptomatic remission over a sufficient follow-up (12 months).

Conditions

Sponsors & Collaborators

Principal Investigators

  • J M AZORIN, Professor · Hopital Sainte Marguerite - MARSEILLE - FRANCE

  • A SOLVET, Doctor · AstraZeneca - FRANCE

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-04-30
Primary Completion
2013-12-31
Completion
2013-12-31

Countries

  • France

Study Locations

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Entities

Diseases
Companies

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 NCT01663974 on ClinicalTrials.gov