Actively Recruiting

Early Phase 1
Age: 16Years - 20Years
All Genders
Healthy Volunteers
ID06636812

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

Age: 16Years - 20Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

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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

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