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Effect of celecoxibe added to sertralin in patients with moderate to severe depression

A double-blind placebo controlled trial of celecoxibe added to sertralin in patients with moderate to severe depression

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT138903124090N1
Enrollment
50
Registered
2010-09-01
Start date
2010-06-15
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 Depression. Severe depressive episode without psychotic symptoms

Interventions

Intervention 1: Case group will receive Serteralin (200 mg/d) + Celexibe (200 mg BID) for 6 weeks. Intervention 2: Control group will receive Serteralin (200 mg/d) + Placebo for 6 weeks.
Placebo
Case group will receive Serteralin (200 mg/d) + Celexibe (200 mg BID) for 6 weeks.
Control group will receive Serteralin (200 mg/d) + Placebo for 6 weeks

Sponsors

National Iranian Oil Company Health Organization
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1. Major Depression according to DSM IV and Hamilton Depression Scale(HamD) 2. 18 y 50 y Exclusion Criteria: 1. Having psychotic disorders 2. Receiving anti-depressant drugs during last month 3. Receiving ECT during last two months 4. Having thyroid disorder 5. Having Cardiovascular disorders 6. Pregnancy 7. Breast Feeding 8. Age 50 y

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Antidepressants and Celxocibe side effects. Timepoint: 0, 2, 4 and 6 weeks intervals. Method of measurement: drug side effects check list.

Primary

MeasureTime frame
Depression. Timepoint: 0, 2, 4, 6 weeks intervals. Method of measurement: Hamilton depression scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactProfessor Shahin Akhondzadeh

Tehran University of Medical Sciences

s.akhond@neda.net+98 912 171 1045

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 26, 2026