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RECRUITINGEarly Phase 1INTERVENTIONAL

Losartan and Emotional Learning

The Effects of Single-dose Losartan on Cognitive Flexibility and Learning in Healthy Adults: a Randomised Controlled Study

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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

Who May Be Eligible (Plain English)

Who May Qualify: - Willing and able to provide willing to sign a consent form - Aged 18-50 years - Score of or below 45 on the Dimensional Anhedonia Rating Scale (DARS; Rizvi et al., 2015) - 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) Who Should NOT Join This Trial: - Past or present DSM-5 axis-I diagnosis (based on SCID results at screening) other than anxiety disorder, dysthymia or unipolar depression - First-degree family member with severe psychiatric illness - CNS-medication last 6 weeks (including as part of another study) - Current blood pressure or other heart medication (especially aliskiren or beta blockers) - 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 consecutive measurements) measures of blood pressure under standardised conditions where either the systolic or the diastolic blood pressure or both are below 90/50 mmHg (in accordance with established standard definitions: DOI 10.1186/s12887-016-0633-7)) - Lifetime history of epilepsy or other neurological disease (e.g. autism, ADHD) - Lifetime history of 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 - Significant loss of hearing that is not corrected with a hearing device - Women: pregnancy, breast-feeding Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Willing and able to provide informed consent * Aged 18-50 years * Score of or below 45 on the Dimensional Anhedonia Rating Scale (DARS; Rizvi et al., 2015) * 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) Exclusion Criteria: * Past or present DSM-5 axis-I diagnosis (based on SCID results at screening) other than anxiety disorder, dysthymia or unipolar depression * First-degree family member with severe psychiatric illness * CNS-medication last 6 weeks (including as part of another study) * Current blood pressure or other heart medication (especially aliskiren or beta blockers) * 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 consecutive measurements) measures of blood pressure under standardised conditions where either the systolic or the diastolic blood pressure or both are below 90/50 mmHg (in accordance with established standard definitions: DOI 10.1186/s12887-016-0633-7)) * Lifetime history of epilepsy or other neurological disease (e.g. autism, ADHD) * Lifetime history of 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 * Significant loss of hearing that is not corrected with a hearing device * Women: pregnancy, breast-feeding

Treatments Being Tested

DRUG

Losartan potassium 50mg

Single dose losartan (50 mg, weight-adjusted), encapsulated identically to placebo

OTHER

Placebo

Single tablet encapsulated identically to losartan

Locations (1)

Warneford Hospital, University of Oxford
Oxford, Oxfordshire, United Kingdom