Clinical Trials Directory

Trials / Completed

CompletedNCT01937013

Impact of Emotional Mimicry and Oxytocin on Frontotemporal Dementia

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
52 (actual)
Sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Academic / Other
Sex
All
Age
30 Years – 85 Years
Healthy volunteers
Accepted

Summary

This study will evaluate the effects on emotions and neural activity of a one time dose of intranasal oxytocin vs. placebo in patients with FTD and healthy controls.

Detailed description

Frontotemporal dementia (FTD) and Pick's disease cause changes in personality, behaviour, and emotional responses. The usual treatments for Frontotemporal dementia focus on reducing agitation and aggressive behaviours. However, these drugs do not help all patients who experience blunting of emotion and loss of empathy. This study will evaluate the effects on emotions and neural activity of a one time dose of intranasal oxytocin vs. placebo in patients with FTD and healthy controls.

Conditions

Interventions

TypeNameDescription
DRUGIntranasal oxytocinOxytocin can be given intravenously (with a needle) or intranasally (a spray into the nose). The intravenous form of drug is approved by Health Canada for use in pregnancy. The intranasal formulation is not currently approved for use by Health Canada, but is used in Europe to induce labour in pregnant women or aid lactation (breastfeeding). Participants will be randomized to receive 72 IU intranasal oxytocin on either study visit 2 or 3.
DRUGSaline Nasal MistParticipants will be randomized to receive placebo on either study visit 2 or 3.

Timeline

Start date
2013-09-12
Primary completion
2017-12-21
Completion
2017-12-21
First posted
2013-09-09
Last updated
2018-08-08

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01937013. Inclusion in this directory is not an endorsement.