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UnknownNCT06034158

Molecular Basis of Loss Aversion

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Sir Run Run Shaw Hospital · Academic / Other
Sex
All
Age
25 Years – 40 Years
Healthy volunteers
Accepted

Summary

The goal of this clinical trial is to test the roles of dopamine and norepinephrine in decision making related to loss aversion in the healthy population. The main question it aims to answer is whether temporarily boosting dopamine activity or temporarily suppressing norepinephrine activity has an impact on processing of potential gains and losses in financial decision making, social decision making, transaction decision making and moral decision making. Accordingly, participants will complete four decision-making tasks, namely investment task, driving task, trading task, and die task, after taking madopar, propranolol or placebo. Participants' psychological traits and psychiatric symptoms will be assessed once they are enrolled before the first-session day.

Conditions

Interventions

TypeNameDescription
DRUGsingle-dose madopar, single-dose propranolol, and single-dose placebo by orderParticipants will take madopar, propranolol, and placebo (orange juice) each once in three separate sessions. The interval between every two sessions will be at least 3 days.
DRUGsingle-dose madopar, single-dose placebo, and single-dose propranolol by orderParticipants will take madopar, placebo(orange juice), and propranolol each once in three separate sessions. The interval between every two sessions will be at least 3 days.
DRUGsingle-dose propranolol, single-dose madopar, and single-dose placebo by orderParticipants will take propranolol, madopar, and placebo(orange juice) each once in three separate sessions. The interval between every two sessions will be at least 3 days.
DRUGsingle-dose propranolol, single-dose placebo, and single-dose madopar by orderParticipants will take propranolol, placebo(orange juice), and madopar each once in three separate sessions. The interval between every two sessions will be at least 3 days.
DRUGsingle-dose placebo, single-dose propranolol, and single-dose madopar by orderParticipants will take placebo(orange juice), propranolol, and madopar each once in three separate sessions. The interval between every two sessions will be at least 3 days.
DRUGsingle-dose placebo, single-dose madopar, and single-dose propranolol by orderParticipants will take placebo(orange juice), madopar, and propranolol each once in three separate sessions. The interval between every two sessions will be at least 3 days.

Timeline

Start date
2023-09-18
Primary completion
2024-03-01
Completion
2024-09-01
First posted
2023-09-13
Last updated
2023-09-26

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06034158. Inclusion in this directory is not an endorsement.