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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04148261
Other study ID # 53325
Secondary ID
Status Withdrawn
Phase Early Phase 1
First received
Last updated
Start date December 2020
Est. completion date December 2022

Study information

Verified date September 2021
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study investigates the effects of two hormones called epinephrine and cortisol on how the brain processes emotional material using functional MRI to measure brain activity. The study hopes to learn how epinephrine and cortisol affect the brain differently in depressed and non-depressed individuals.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2022
Est. primary completion date December 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 55 Years
Eligibility Inclusion Criteria: - Weight of less than 280 pounds - HAM-D Score of greater than 7 for depression participants Exclusion Criteria: - Psychotropic medications - Recent surgery - Endocrine disorders - Liver disease - Kidney disease - Thyroid disorder - History of malaria - Tuberculosis - Osteoporosis - Glaucoma or cataracts - Chronic expressed infections (herpes, HIV, etc) - History of congestive heart failure - History of recurring seizures - Stomach ulcers - Comorbid psychosis - Current use of illicit drugs - Diabetes - Any cardiovascular disease (angina, hypovolemia, coronary artery disease, low/high blood pressure, etc) - Any pulmonary disease - Any cerebrovascular disease - Sulfate hypersensitivity - Glaucoma - Infection - Pregnancy - Parkinson's Disease - Panic Disorder - Over 280 pounds in weight - In-dwelling ferrous metals - Left handed - Abnormal hearing - Claustrophobic - Head injury with loss of consciousness - Active suicidal ideation

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Hydrocortisone Acetate (CORT)
Participants will receive a single dose of hydrocortisone at a dosage of 0.65 mg/kg
Epinephrine Sulfate (EPI)
Participants will receive a continuous infusion of epinephrine at a dosage of 80 ng/kg/min
Placebo (PLB)
Participants will receive a placebo

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Outcome

Type Measure Description Time frame Safety issue
Primary Sadness-induced subgenual cingulate activity as measured by functional magnetic resonance imaging 2 hours
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