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NCT05262868: rTMS-PSYGER

rTMS for the Treatment of Affective Symptoms in Patients Suffering From Dementia

Status unknown Phase 4 Last updated 2 March 2022
What this trial tests

Phase 4 trial testing rTMS in Behavioral and Psychiatric Symptoms of Dementia in 44 participants. Status unknown.

Timeline
1 January 2022
Primary endpoint
31 October 2023
31 January 2024

Quick facts

Lead sponsorCentre Hospitalier Universitaire Vaudois
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment44
Start date1 January 2022
Primary completion31 October 2023
Estimated completion31 January 2024
Sites1 location across Switzerland

Drugs / interventions tested

Conditions studied

Sponsor

Centre Hospitalier Universitaire Vaudois

Who can join

65 and older, any sex, with Behavioral and Psychiatric Symptoms of Dementia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of rTMS

Trials testing the same drug.

Other recruiting trials for Behavioral and Psychiatric Symptoms of Dementia

Currently open trials in the same condition.

Other Centre Hospitalier Universitaire Vaudois trials

Trials by the same sponsor.

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Data sources for this page

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