Viewing Study NCT05262868


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Ignite Modification Date: 2025-12-24 @ 5:37 PM
Study NCT ID: NCT05262868
Status: UNKNOWN
Last Update Posted: 2022-03-02
First Post: 2022-02-21
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: rTMS for the Treatment of Affective Symptoms in Patients Suffering From Dementia
Sponsor: Centre Hospitalier Universitaire Vaudois
Organization:

Study Overview

Official Title: Repetitive Transcranial Magnetic Stimulation (rTMS) for the Treatment of Affective Symptoms in Patients Suffering From Dementia: a Randomised Clinical Trial
Status: UNKNOWN
Status Verified Date: 2022-02
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: rTMS-PSYGER
Brief Summary: This is a monocentric prospective, randomized, double-blind placebo-controlled study. It is designed to evaluate the superiority of the rTMS over sham treatment of depressive symptoms in the context of dementia. It is aimed at a population ≥ 65 years old, with affective BPSD. We wish to recruit 44 participants, with an estimated rate of potential drop out of 20%. Patients will be randomly assigned to the sham or rTMS group. The sham stimulation reproduces the procedure in all the steps, has the same duration and differs exclusively by the device setting. After inclusion, both groups will receive 15 sessions distributed over 5 days a week for 3 weeks
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: