Phase
Condition
N/ATreatment
Losartan potassium 50mg
Placebo
Clinical Study ID
Ages 18-50 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Willing and able to provide informed consent
Aged 18-50 years
Sufficient written and spoken English skills to understand what the study involves,and to complete the questionnaires
Non- or light-smoker (5 cigarettes a day, if vaping: less than 50 puffs)
BMI between 18 - 30
Exclusion
Exclusion Criteria:
Current DSM-5 axis-I diagnosis (based on SCID results at screening) or history of asevere psychological disorder such as psychotic disorder, bipolar disorder, alcoholor substance abuse, or post-traumatic stress disorder
First-degree family member with severe psychiatric illness (including psychosis,bipolar disorder, unipolar psychotic depression).
CNS-medication last 6 weeks (including as part of another study)
Current blood pressure or other heart medication, including aliskiren and betablockers)
Diagnosis of intravascular fluid depletion or dehydration
History of angioedema
Impaired kidney function (based on self-report)
Very low blood pressure (defined as repeated (at least three consecutivemeasurements) measures of blood pressure under standardised conditions where eitherthe systolic or the diastolic blood pressure or both are below 90/50 mmHg (inaccordance with established standard definitions)
Lifetime history of epilepsy or other neurological disorder, as established by aprofessional diagnosis (e.g. autism, ADHD)
Lifetime history of systemic infection, or clinically significant hepatic, cardiac,obstructive respiratory, renal, cerebrovascular, metabolic, endocrine or pulmonarydisease or disorder which, in the opinion of the investigator, may either put theparticipants at risk because of participation in the study, or may influence theresult of the study, or the participant's ability to participate in the study
Significant loss of hearing that is not corrected with a hearing device
Women: pregnancy (as determined by a urine test, if the participant's pregnancystatus is unknown during the in-person visit), breast-feeding
Study Design
Study Description
Connect with a study center
Warneford Hospital
Oxford, Oxfordshire OX37JX
United KingdomSite Not Available
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