Actively Recruiting
The Effects of Single-dose Losartan on the Processing of Emotional Information in Healthy Adolescents: a Randomised Controlled Study
Led by University of Oxford ยท Updated on 2025-06-15
60
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Oxford
Lead Sponsor
N
National Institute for Health Research, United Kingdom
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying how a single dose of losartan, a blood pressure medication, affects emotional processing in healthy young people aged 16 to 20 years. Adolescents often have difficulty with fear extinction, a process related to overcoming anxiety, and this study aims to understand if losartan can improve this by enhancing brain function in areas involved in emotion regulation. The trial is randomized and double-blind, meaning neither participants nor researchers know who receives losartan or placebo during the study. Participants will receive one dose of losartan adjusted by weight (50mg if over 50kg, 25mg if below) or a placebo capsule. One hour after taking the capsule, when the drug reaches peak levels in the body, they will complete various computerized tests. These tests include a fear extinction task and others that assess attention and learning from emotional and neutral stimuli. The study evaluates the drug's impact on emotional and cognitive functions relevant to anxiety. During the study, participants will undergo assessments one hour after capsule intake, including measures of fear extinction, pattern separation, cognitive flexibility, reinforcement learning, and attention to faces. The trial is conducted with healthy volunteers and will monitor safety and effects throughout. The total participation involves attending appointments in Oxford, completing tasks, and providing consent and contact details for follow-up. The study's results may help improve understanding of anxiety treatments for adolescents.
CONDITIONS
Brief Title
Losartan and Emotional Processing in Young People
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Willing and able to provide informed consent (for ages 16 and 17: assent plus parental or legal guardian consent)
- Non-smoker or light smoker (less than 5 cigarettes per day)
- Able to attend study appointments in Oxford with reasonable travel costs
- Willing and able to provide general practitioner contact details
You will not qualify if you...
- Past or current severe psychiatric illness or alcohol/substance dependence
- First-degree family member with severe psychiatric illness
- Use of central nervous system medication in the past 6 weeks
- Current blood pressure or heart medication use
- Diagnosis of intravascular fluid depletion or dehydration
- Impaired kidney function
- Significant high potassium levels
- Very low blood pressure (repeated measures below 90/50 mmHg)
- Body weight below 35 kg
- History of epilepsy or other neurological disorders
- History of angioedema, renal artery stenosis, valvular heart disease, or recurrent orthostatic hypotension
- Significant systemic infections or serious organ diseases
- Significant hearing loss not corrected with a device
- Insufficient English language skills
- Pregnancy or breastfeeding for women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single day
Participants receive a single dose of losartan or placebo, followed by computerized tasks assessing emotional processing one hour later.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Warneford Hospital, University of Oxford
Oxford, Oxfordshire, United Kingdom, OX37JX
Actively Recruiting
Research Team
A
Andrea Reinecke, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here