CTRI/2018/06/014537
Recruiting
未知
A prospective, observational study to assess the effects of SSRI and SNRI on cognitive function in patients of Major Depressive Disorders (MDD)
Department of Pharmacology IPGMER0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- All adult diagnosed patients of MDD as per ICD 10 criteria in remission phase
- Sponsor
- Department of Pharmacology IPGMER
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\)Adult patients (18 years to 50 years) of either gender attending psychiatry OPD at IOP,
- •with a clinical diagnosis of Major Depressive Disorder as per ICD10 criteria.
- •2\)Subjects of MDD must be in remission phase with a Hamilton Depressive Rating Score (HAM\-D 17\) of \<7\) at enrolment and taking any of the following SSRIs \- fluoxetine, sertraline, escitalopram and/or SNRI like mirtazapine for at least last 6 months. Patients who are additionally on cognitive behavioral therapy (CBT) as part of their treatment shall also be included.
- •3\)Subjects should have at least 8 years of formal school education in order to undertake the cognitive function tests.
- •4\)Subjects or their care givers should be willing to give written informed.
Exclusion Criteria
- •1\)History of post traumatic or Obsessive compulsive Disorder (OCD)
- •2\)History of schizophrenia, psychosis or bipolar delusional disorder
- •3\)History of intake of any drugs that are likely to have effect on cognition (anticonvulsants, sedative hypnotics, neuroleptics, opioids)
- •4\)History of addictions\- alcohol, substance abuse
Outcomes
Primary Outcomes
Not specified
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