Skip to content

Cilostazol for the treatment of depression in cardiac patients

Cilostazol for depressive disorder after percutaneous coronary intervention or coronary-artery bypass grafting: A randomized, double-blind, placebo-controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090117001556N154
Enrollment
50
Registered
2023-11-05
Start date
2023-12-22
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

depressive disorder. depressive disorder, single episode

Interventions

Intervention 1: Control group: placebo for 6 weeks. Intervention 2: Intervention group: Cilostazol (100 mg per day) for 6 weeks.

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with coronary artery disease who underwent elective percutaneous coronary intervention or coronary-artery bypass grafting in the past three months due to angina pectoris or left ventricular dysfunction not associated with myocardial infarction. Diagnosis of major depressive disorder based on DSM-V (score between 14 and 17). Age between 40-60.

Exclusion criteria

Exclusion criteria: Patients who have taken antipsychotic drugs in the last year. Diagnosis of other psychiatric disorders. Electroconvulsive treatment in the last two months. History of thyroid disease. Inflammatory diseases, including autoimmune thyroiditis, inflammatory bowel disease, systemic lupus erythematosus, psoriasis, autoimmune hepatitis, migraine, Guillain-Barre syndrome, multiple sclerosis, and rheumatoid arthritis. Being pregnant or breastfeeding. History of allergy to Cilostazol. Simultaneous need for antithrombin alpha, antithrombin III, argatroban, enoxaparin, apixaban, and other drugs with severe interaction with Cilostazol.

Design outcomes

Primary

MeasureTime frame
Severity of depression. Timepoint: Weeks: 0-2-4-6. Method of measurement: By Hamilton Depression Rating Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Shahin Akhondzadeh

Tehran University of Medical Sciences

s.akhond@sina.tums.ac.ir+98 21 5541 2222

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026