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Dissecting the mechanisms of fear formation: a pharmacological study with healthy volunteers

Dissecting the mechanisms of fear formation: a pharmacological study with healthy volunteers - camf

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON38140
Enrollment
120
Registered
2011-06-30
Start date
2012-05-01
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

post-traumatic stress disorder PTSD

Interventions

In this study we will make use of the pharmacological agents atomoxetine, propranolol and placebo in a randomized double blind design in order to probe the effects of the differential neurotransmitt

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: The subjects must be in good mental and physical health (as established by first contact and health questionnaire). Participants with a past or present psychiatric,or respiratory (including asthma) will be excluded from the study. Background of high blood pressure or cardiovascular diseases will also be an exclusion criterion. Testing days for female subjects will demand that they are in the end of the follicular phase in order to standardize the influence of gonadal hormones. Participants must be drug and alcohol free from at least 48 hrs before time of testing and should refrain from caffeine and cigarette smoking from 3 hours before testing. Age should be comprised between 18 and 40 years.

Exclusion criteria

Exclusion criteria: Uncorrected vision disturbances, pregnancy, use of oral contraceptives or lactation, any neurological and psychiatric diseases past and present, including manic and suicidal depression.History of seizures, respiratory disease (including asthma), cardiovascular illness or head trauma with loss of consciousness, abnormal blood pressure, glaucoma or abnormal clinical laboratory tests. Subjects will also be excluded when they cannot understand the Dutch and English languages sufficiently to understand the purposes and implications of the experiment.

Design outcomes

Primary

MeasureTime frame
• Skin conduction response and/or eye blink response as a measure of differential acquisition of memory for each group. • Comparison of fear response measures between the different drug groups and placebo will allow to determine what is the roles of noradrenaline enhancement or blockage in fear memory consolidation. Enhancement or weakening of memory with any of the drugs will allow confirmations of assumptions on the specific effects of noradrenaline in the postlearning consolidation processes.

Secondary

MeasureTime frame
Heart rate data will be used as an auxiliary measure.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)