Actively Recruiting

Early Phase 1
Age: 16Years - 20Years
All Genders
Healthy Volunteers
NCT06636812

Losartan and Emotional Processing in Young People

Led by University of Oxford · Updated on 2025-06-15

60

Participants Needed

1

Research Sites

94 weeks

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

This study explores the effects of single-dose losartan (50mg) versus placebo on emotional processing in young healthy volunteers.

CONDITIONS

Official 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 give informed consent (for ages 16-17: assent plus parental or guardian consent)
  • Non-smoker or light smoker (fewer than 5 cigarettes daily)
  • Able to attend study visits in Oxford with reasonable travel costs
  • Willing and able to provide general practitioner contact details
Not Eligible

You will not qualify if you...

  • Any past or current DSM-5 axis-I psychiatric diagnosis, especially severe illness or substance dependence
  • First-degree relative with severe psychiatric illness
  • Use of central nervous system medication in the last 6 weeks
  • Current use of blood pressure or heart medication, including aliskiren or beta blockers
  • Diagnosis of dehydration or fluid depletion
  • Kidney impairment (eGFR below 75 ml/min/1.73 m2)
  • Significant high potassium levels (hyperkalaemia)
  • Very low blood pressure (repeated readings below 90/50 mmHg)
  • Body weight below 35 kg
  • History of epilepsy or neurological disorders such as ADHD or autism
  • History of angioedema, renal artery stenosis, heart valve disease, or recurrent orthostatic hypotension
  • History of serious infections or major liver, heart, lung, kidney, metabolic, endocrine, or brain disorders that could affect safety or study results
  • Significant hearing loss not corrected by a hearing device
  • Insufficient English language skills
  • Women who are pregnant or breastfeeding

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

CONTACT

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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