RecruitingNCT06697847
Sweet Thresholds in Healthy Volunteers Study
Assessing Taste Thresholds and Scores on Standardised Mood Questionnaires in Participants Without Mood Disorders
Sponsor
Ranvier Health Ltd
Enrollment
30 participants
Start Date
Nov 27, 2024
Study Type
OBSERVATIONAL
Conditions
Summary
The sweet threshold (concentration of sucrose in water) at which healthy participants can detect a sweet flavour will be recorded.
Eligibility
Min Age: 18 Years
Inclusion Criteria7
- Male and female adults of 18 years old and over;
- Participants without a diagnosis of major depressive disorder (MDD) / anxiety disorder;
- Participants not taking an antidepressant during the preceding 6 months
- Not suffering from significant other mental or physical illness, such as confirmed psychosis, end of life care, or any other condition assessed as significant by the Site Investigator;
- Willing and able to comply with all study-related procedures;
- Not having COVID 19 or continuing effects of COVID 19 including altered sense of taste;
- Understands the study requirements and the treatment procedures and is able to provide written informed consent.
Exclusion Criteria8
- Taking antidepressant medication currently or during the previous 6 months;
- Known or suspected hypersensitivity or intolerance to any taste testing solutions, or any of their excipients;
- A history or presence of neurological or confounding psychiatric conditions (such as stroke, traumatic brain injury, epilepsy, space occupying lesions, multiple sclerosis, Parkinson's disease, vascular dementia, transient ischemic attack, or schizophrenia);
- Patients with a diagnosis of chronic pain;
- Pregnancy or possibility pregnancy, or breastfeeding;
- Participants using supplements containing psychoactive herbs (for example St Johns Wort or 5-HTP (5-Hydroxytryptophan, also known as oxitriptan);
- Participants regularly using psychoactive stimulants (for example MDMA);
- Participants unable or unwilling to comply with study procedures.
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Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06697847