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Antidepressant effects of Celecoxib in the treatment of patients with colon cancer

celecoxib in the treatment of mild to moderate depression in patients with colon cancer: A randomized placebo controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201508201556N79
Enrollment
40
Registered
2015-08-23
Start date
2015-08-23
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. Major Depressive episode

Interventions

Intervention 1: Capsule Celecoxib200 mg BID as intervention group for 6 weeks. Intervention 2: Cap. placebo as control group for 6 weeks.
Treatment - Drugs
Placebo
Capsule Celecoxib200 mg BID as intervention group for 6 weeks

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1-Confirmation of colon cancer;2-receiving chemotherapy 3- score lower than 20 in Hamilton Rating Scale for depression 4-Mild to moderate major depressive disorder based on DSM-5 Exclusin criteria: 1-psychosis or other psychiatric disorder 2-Receiving psychotropic medications,3- receiving any antidepressants during past one month or ECT during past two months 4-history of cardiovascular disease , 5-pregnancy or breast feeding, 6-thyroid diseases

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of depression. Timepoint: Baseline and weeks 2-4-6 after beginig of treatment. Method of measurement: by Hamiltion Depression Rating Scale 17-Item.

Secondary

MeasureTime frame
Severity of pain. Timepoint: Baseline and weeks 2-4-6 after beginig of treatment. Method of measurement: by Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactProf. 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