Clinical Trials Directory

Trials / Completed

CompletedNCT06200883

Effects of a Nutraceutic Compound on Cognitive Impairment

Effects of a Nutraceutic Compound on Cognitive Impairment in Frailty Patients

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
58 (actual)
Sponsor
Federico II University · Academic / Other
Sex
All
Age
40 Years
Healthy volunteers
Not accepted

Summary

The study is designed to evaluate the effects of choline bitartrate on cognitive impairment in frailty patients. The study will analyze the impact of 4 weeks treatment randomized with a nutraceutical compound in a double-blind randomized placebo controlled trial. The investigators will also assess cognitive frailty.

Detailed description

The patients and controls will be recruited at the Hypertension research center of Federico II university hospital. The overall duration of the study will be 4 weeks for each participant. Blood pressure, heart rate and cognitive frailty and cognitive impairment will be evaluated for each patient at randomization and after 4 weeks of treatment. Patients or controls will be randomized to receive the nutraceutical compound (1 vial of CEREBRAIN per os with 1200 mg of choline bitartrate every 24 hours) or placebo (1 vial per os without active substance every 24 hours). Before the start of treatment, patients will undergo full examination of cognitive functions (MoCA and MMSE tests, the parameters will be reported in a password-protected database, using a identification code. The duration of the treatment will be 4 weeks. At the end of the treatment, the patients will repeat the tests and the results will be identified through the use of an alphanumeric code (POST-XXXYYY). All CEREBRAIN and placebo, made up of the CEREBRAIN vehicle without the active substance, will be offered free of charge by the Farmaceutici DAMOR company.

Conditions

Interventions

TypeNameDescription
DRUGPlacebo oral vialIn the Placebo group the participants take vehicle (1 vial per os every 24 hours) for 4 weeks
DRUGCholine BitartrateIn the CEREBRAIN group the participants take CEREBRAIN (1 vial per os of 1.2 g every 24 hours) for 4 weeks

Timeline

Start date
2022-09-01
Primary completion
2023-09-01
Completion
2023-11-01
First posted
2024-01-11
Last updated
2024-01-11

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT06200883. Inclusion in this directory is not an endorsement.

Effects of a Nutraceutic Compound on Cognitive Impairment (NCT06200883) · Clinical Trials Directory