Overview

The Effect of Losartan on Emotional Processing in Healthy Volunteers

Status:
Completed
Trial end date:
2017-06-30
Target enrollment:
0
Participant gender:
All
Summary
This experimental medicine study explores whether a single dose of losartan (50mg) versus placebo affects the processing of positive and negative stimuli, using fMRI.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
University of Oxford
Treatments:
Losartan
Criteria
Inclusion Criteria:

- willing and able to provide informed consent

- male or Female, aged 18-50

- body mass index (BMI) of 18-30 kg/m2

- fluent English skills

- non- or light-smoker (< 5 cigarettes a day)

Exclusion Criteria:

- Female participant who is pregnant or breast-feeding

- central nervous system (CNS) active medication during the last 6 weeks

- Current blood pressure/other heart medication (esp. aliskiren or beta blockers)

- Intravascular fluid depletion

- Past or present DSM-IV (Diagnostic and Statistical Manual of Mental Disorders) axis-I
diagnosis

- Alcohol or substance abuse

- First-degree family member with a history of a severe psychiatric disease

- Impaired liver or kidney function

- Lifetime history of epilepsy or other neurological disease, systemic infection, or
clinically significant hepatic, cardiac, obstructive respiratory, renal,
cerebrovascular, metabolic, endocrine or pulmonary disease or disorder which, in the
opinion of the investigator, may either put the participants at risk because of
participation in the study, or may influence the result of the study, or the
participant's ability to participate in the study.

- Insufficient English skills

- participated in another study involving certain medication during last 6 weeks

- Contraindication to magnet resonance imaging (MRI) scanning (e.g. pacemaker)