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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04717921
Other study ID # Mehmet Diyaddin Güleken
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date September 1, 2020
Est. completion date September 1, 2021

Study information

Verified date March 2021
Source Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to assess the changes in retinal nerve fiber layer due to SSRI treatment in first-attack major depressive patients.


Description:

Selective serotonin reuptake inhibitors (SSRIs) are among the most used and safe antidepressant drugs in the world. In previous studies, SSRIs have been found to cause an increase in brain gray matter volume in patients with major depression (MD). Optical coherence tomography (OCT) is a non-invasive medical imaging method that displays biological tissue layers by taking high-resolution tomographic sections. Changes in the thickness of the retinal nerve fiber layer (RNFL), a layer of the ganglion cell complex in the retinal layer of the eye and composed of ganglion cell axons, occur due to axonal damage in the retinal nerve tissue. Since RNFL is similar to brain gray matter tissue, recently neurological and psychiatric studies have been conducted to provide data on the neurodegeneration that occurs in the brain by OCT. However, in a recent cross-sectional study, contrary to what was expected, thinning of the retinal nerve fiber layer was detected in psychiatric patients using SSRI drugs compared to the healthy group, and this was attributed to a probable maculopathy caused by SSRIs in the eye. In this study, it is aimed to assess the probable cortical volume changes of the patients by measuring the changes in retinal nerve layers due to SSRI treatment in first-attack MD patients.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 60
Est. completion date September 1, 2021
Est. primary completion date May 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - First attack depressive patients between 18 and 65 years - Diagnosed with the Structured Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders 5 / Clinical Version (SCID-5 / CV) - Started to be treated with selective serotonin reuptake inhibitors - Having a Standardized Mini Mental Test (SMMT) score of 24 or more and - Healthy subjects with no psychiatric history, having a SCL-90-R (GSI) score of less than 1.0 Exclusion Criteria: - Depressive subjects with any neurological (cerebrovascular disease, head trauma, intracranial mass, dementia, epilepsy, multiple sclerosis, etc.) or general medical (such as diabetes, hypertension, myocardial infarction, etc.) diagnosis, with an ocular surgery or a history of ocular trauma, retinal pathology (detachment, etc.), other eye pathologies such as optic nerve neuropathy and refractive error, previous history of antidepressant drug use, alcohol-substance abuse or addiction, - Healthy individuals with a history of psychiatric diagnosis or a SCL-90-R (GSI) score of 1.0 or above

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Saglik Bilimleri Üniversitesi Gazi Yasargil Tranining and Research Hospital Diyarbakir

Sponsors (1)

Lead Sponsor Collaborator
Mehmet Diyaddin Güleken

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Retinal nerve fiber layer thickness Retinal nerve fiber layer thickness change during selective serotonin reuptake inhibitor treatment in first attack depressive subjects Baseline, at first week and at the 8th week of the treatment
Secondary Choroid thickness Choroid thickness change during selective serotonin reuptake inhibitor treatment in first attack depressive subjects Baseline, at first week and at the 8th week of the treatment
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