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2025-520899-25-00RecruitingPhase 4

PILOT STUDY ON THE EFFECTIVENESS OF CHOLINE ALFOSCERATE IN THE UNDER THRESHOLD DEPRESSION OF THE ELDERLY

Source: EU CTIS (euclinicaltrials.eu) · Last updated 22 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Next steps

Brief summary (registry, in English)

The primary objective of the study is to evaluate the efficacy of choline alfoscerate on subthreshold depression in elderly patients.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
20 (estimated)
First submitted
28 Jan 2025
Start date
17 May 2024
Lead sponsor
Azienda Socio Sanitaria Territoriale Di Lodi
Diseases
Depression
EU CT number
2025-520899-25-00
EudraCT number
2021-003437-10

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 20
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any contraindication to treatment or intolerance to choline alfoscerate 2. Diagnosis of Major Depressive Episode or Dysthymia 3. Diagnosis of Schizophrenia or other psychotic disorders, Bipolar Disorder or Dementia 4. Alcohol / drug / substance abuse or dependence 5. Severe organic disease (eg major surgery, metastatic cancer, stroke, severe neurological disorder, myocardial infarction, chronic heart failure) 6. Treatment with antidepressants or psychotherapy within 2 weeks prior to recruitment 7. Any condition which, in the opinion of the investigator, might put the patient at risk by participation in this study 8. Patients involved in other clinical trials

Who the study is looking for

  • Age = 65 years 2. From 2 to 4 depressive symptoms present for at least two weeks prior to enrollment (Judd et al., 1994) 3. Mini-Mental State Examination (MMSE) score = 24 4. Montreal Cognitive Assessment (MOCA) score < 26 5. Patients able to understand and sign informed consent 6. Informed consent signature

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

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Azienda Socio Sanitaria Territoriale di LodiLodiItalyRecruiting

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