Actively Recruiting

Age: 18Years +
All Genders
ID07078227

5 Years Follow-up of the Study: Pharmacogenetics in Depressed Patients with Focus on Difficult-to-Treat Depression, Suicide Attempt, and CYP2D6

Led by Region Skane · Updated on 2026-04-30

415

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

Sponsors

R

Region Skane

Lead Sponsor

L

Lund University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating the long-term outlook and factors predicting treatment results for people with difficult-to-treat depression under secondary psychiatric care. This study follows a group of 415 patients originally studied between 2012 and 2021, who were carefully assessed for their diagnosis and previous treatments. All participants were genotyped for enzymes CYP2D6 and CYP2C19, and blood samples were stored for further analysis related to prognosis. The current study involves a five-year follow-up of these patients through review of medical records and national register data. No new treatments or interventions are provided during this period. Data collected will include information on suicide attempts, hospital visits, treatments received, personality assessments, and clinical improvements. The study aims to examine symptom patterns, the clinical course of depression, suicidality, and the impact of earlier pharmacological counseling offered to some participants. Participants' involvement consists of allowing access to their medical and registry data for a period of five years after the original study. Researchers will track clinical outcomes such as suicide attempts, depression progression, personality disorder diagnoses, bipolar disorder characteristics, and biomarker effects. The study uses approved opt-out consent, where participants can decline but are otherwise included. The total follow-up period is five years from each participant's baseline enrollment in the original study.

CONDITIONS

Brief Title

Long-term Follow-up of Depressive Disorders in Psychiatric Care

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Participation in the study "Pharmacogenetics in depressive patients with specific focus on difficult-to-treat depression, suicide attempt and CYP2D6"
Not Eligible

You will not qualify if you...

  • Not wanting to participate in the follow-up study

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or digital)

Long-term Monitoring

Duration - 5 years

Participants are observed for long-term prognosis of depression through medical records review and registry data extraction without active intervention.

Data collection based on medical records and registers; no in-person visits required

Trial Site Locations

Total: 2 locations

1

Psychiatry Reserach Unit

Lund, Sweden, 221 85

Active, Not Recruiting

2

Research Unit, Office of Psychiatricy, habilitation and technical aid

Lund, Sweden, 221 85

Actively Recruiting

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Research Team

M

Marie Asp, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

Recognition of personality disorder and anxiety disorder comorbidity in patients treated for depression in secondary psychiatric care.

Marie Asp, Daniel Lindqvist, Johan Fernström...

https://pubmed.ncbi.nlm.nih.gov/31895938