Outcomes Associated With Suicidality in Inpatients With Symptoms of Depression (OASIS-D)

NCT04404309 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 3331

Last updated 2024-02-07

No results posted yet for this study

Summary

This 6-month, naturalistic cohort study examines male and female inpatients aged 18 to 75 years i) with any form of unipolar depressive episode (cohort 1); ii) clinical diagnosis of a moderate or severe unipolar depressive episode and suicidal tendencies who agree to participate in a prospective study (cohort 2); and moderate or severe unipolar depressive episodes validated by research interviews and and suicidal tendencies that persist for at least 48 hours after admission who are followed up for 6 months (cohort 3).

Conditions

Sponsors & Collaborators

  • Janssen-Cilag G.m.b.H

    collaborator INDUSTRY
  • Charite University, Berlin, Germany

    lead OTHER

Principal Investigators

  • Christoph U Correll, MD · Charite University, Berlin, Germany

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-01
Primary Completion
2024-12-31
Completion
2024-12-31

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 NCT04404309 on ClinicalTrials.gov