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Aspirin as an augmenting to Sertraline for treating major depressive disorder, a randomized double blind placebo controlled clinical tria

Aspirin as an augmenting to Sertraline for treating major depressive disorder, a randomized double blind placebo controlled clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016082829556N1
Enrollment
100
Registered
2016-10-10
Start date
2016-09-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Major Depressive Disorder. Depressive episode

Interventions

Intervention 1: Sertraline as a serotonin reuptake inhibitor with 150mg daily dosing for 8 week and is production of Dr Abidi pharmacy. and Aspirin (acetyl salysilic acid) 80mg two times per day for 8
Treatment - Drugs
Placebo
Sertraline as a serotonin reuptake inhibitor with 150mg daily dosing for 8 week and is production of Dr Abidi pharmacy + placebo for 8 week
Sertraline as a serotonin reuptake inhibitor with 150mg daily dosing for 8 week and is production of Dr Abidi pharmacy. and Aspirin (acetyl salysilic acid) 80mg two times per day for 8 week that is pr

Sponsors

Vice chancellor for research of Kashan University of Medical Sciences and Health Servisces,Kashan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with major depressive disorder according to DSM-VI, both gender, and aged between 40 and 80 years old, Consent to participate in the study by completing the informed consent form, Having risk factors for coronary heart disease or stroke. Exclusion criteria: Depression due to physical illness or drug use, A history of gastric ulcers and contraindications for taking aspirin, pregnant women, History of alcohol and substance abuse within 6 months prior to the beginning of the study, positive history of mania, mental retardation, psychosis, using another antidepressant within 4 weeks prior to starting ASA, Candidates for other treatments such as ECT for depression.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Depression. Timepoint: baseline,4 week, and8 week. Method of measurement: Beck Depression Inventory.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Fahimi

Kashan University of Medical Sciences and Health Services

hossein1fahimi@gmail.com+98 31 5531 4908

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 8, 2026