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Trials / Withdrawn

WithdrawnNCT01667744

Citalopram for Sx/Util in Acute Coronary Syndrome Patients

Status
Withdrawn
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Henry Ford Health System · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Symptoms (chest pain, shortness of breath, dizziness, etc.) and treatment usage (doctor or emergency room visits, testing, hospital days, etc.) in patients with Acute Coronary Syndromes are known to be related to emotional distress (Anxiety, Depression and Anger). In addition, behavioral treatment of emotional distress is known to decrease symptoms, and treatment usage. The present protocol tests whether the addition of a medication known to reduce emotional distress can also reduce symptoms and treatment usage. This will done by recruiting patients with ACS during their hospital stay, randomizing them to receive citalopram or placebo, and then examining their symptoms and treatment usage at 6 months.

Detailed description

Not applicable. Study not funded.

Conditions

Interventions

TypeNameDescription
DRUGCitalopram10 mg/day

Timeline

Start date
2016-01-01
Primary completion
2016-02-01
Completion
2021-02-16
First posted
2012-08-17
Last updated
2022-12-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01667744. Inclusion in this directory is not an endorsement.

Citalopram for Sx/Util in Acute Coronary Syndrome Patients (NCT01667744) · Clinical Trials Directory