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Clinical Trials/IRCT20090117001556N125
IRCT20090117001556N125
Not yet recruiting
Phase 2

Studying the effects of Celecoxib as monotherapy in the treatment of postpartum depression with mild intensity to the average: response to treatment of Celecoxib by area Brain-Derived Neurotrophic Factor (BDNF) and inflammatory cytokines (TNFa, IFN? , IL-1?, IL-1? IL-6, IL-8)

Tehran University of Medical Sciences0 sites50 target enrollmentStarted: TBDLast updated:

Overview

Phase
Phase 2
Status
Not yet recruiting
Enrollment
50

Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 45 years (—)
Sex
Female

Inclusion Criteria

  • Age between 18 to 45
  • Having mild to moderate depression according to Hamilton Depression Rating Scale (HAM\-D)

Exclusion Criteria

  • Having severe depression according to Hamilton Depression Rating Scale (HAM\-D or HDRS)
  • Addiction to drugs
  • Addiction to alcohol
  • Presence of Thyroid disease
  • Receiving any antidepressant medications during past one month prior to the trial
  • Receiving Electroconvulsive therapy during past two months prior to the trial
  • Any other diagnosis according to axis\-1, DSM\-5
  • Having a risk of suicide based on doctor's clinical judgement or having a score of \>2 in suicide item of Hamilton Depression Rating Scale (HAM\-D or HDRS)
  • Concomitant use of medications that increase the risk of gastrointestinal bleeding
  • Presence of cardiovascular disease

Investigators

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