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NCT06496087Completed

Evaluation of DEPREXIL in Patients With Clinical Depression Through Psychological and Neuroendocrine Assessment

Evaluation of DEPREXIL Treatment in Patients With Clinical Depression Through Psychological and Neuroendocrine Assessment

Source: ClinicalTrials.gov · Last updated 11 Jul 2024

Brief summary (registry, in English)

Clinical depression is a mood disorder that affects people of all ages with symptoms such as sadness, anger or frustration, appetite changes, difficulty concentrating and suicidal thoughts. Psychological and pharmacological treatments are available to treat it, such as cognitive behavioral therapy and antidepressants. Deprexil® from Catalysis is a food supplement that regulates neuronal metabolism and calcium homeostasis, which may help in cases of mild to moderate depression. It is proposed to conduct a study in patients with primary, secondary or post-COVID-19 depression to evaluate the effects of this supplement on psychological and neuroendocrine changes.

Status (registry)
Completed
Study type
Interventional
Enrollment
100 (actual)
First submitted
5 Jun 2024
Start date
1 Nov 2022
Primary completion date
15 Dec 2023
Lead sponsor
Catalysis SL
NCT number
NCT06496087

What you commit to

  • Study type: Interventional
  • Participants enrolled: 100
  • From 1 Nov 2022 to the primary completion date, 15 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients with severe depression requiring antidepressant medication.

Other illness

  • Patients with psychological disorders in addition to depression, such as anxiety, attention deficit, hyperactivity disorder, post-traumatic stress disorder other than that caused by COVID-19, bipolar disorder or other mental disorders secondary to depression.

Other

  • Patients who ingest psychoactive substances.

Who the study is looking for

  • Patients with clinical depression diagnosed primary or secondary to concomitant illness or post COVID-19.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fundación CR INVESTIGATION INSTITUTE
Coordinator of this site? Confirm its status
BogotáColombiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.