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The Efficacy of Early Screening and Treatment of Depression with Selective Serotonin Reuptake Inhibitor (SSRI) in Adult Glioma Patient

Not Applicable
Withdrawn
Conditions
Neoplasms
Registration Number
KCT0005453
Lead Sponsor
Asan Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Withdrawn
Sex
All
Target Recruitment
112
Inclusion Criteria

1)Understand and voluntarily sign an informed consent document prior to any study related assessment/procedures are conducted
2)First time histologically confirmed diagnosis of glioma (resection or biopsy)
3)Age =18 years and = 85 years
4)Glasgow Coma Score (GCS) 5-15

Exclusion Criteria

1)Unable to perform the screening test due to the neurologic deficit
2)Evidence of ongoing acute brain bleeding on CT or MRI
3)Previously confirmed diagnosis of a benign, low- or high-grade brain tumor
4)Diagnosis of systemic cancer other than glioma (breast cancer, lung cancer, gastric cancer, colon cancer etc.)
5)Currently taking antidepressant drugs
6)Previously suffered from depression in the past or within 5 years of diagnosis, and currently do not receive drug therapy
7)Taking following drugs: MAO (monoamine oxidase) inhibitor, linezolid, thioridazine, mesoridazine, pimozide, tizanidine, terfenadine, astemizole or cisapride
8)SSRI allergic history
9)On antiplatelets or anticoagulation agents (aspirin, clopidogrel, cilostazol, heparin, warfarin ?vitamin K antagonist?, DOAC ?Direct Oral Anticoagulants?)
10)On non-steroidal anti-inflammatory drug (NSAID)
11)High bleeding risk patients: hematologic disorder, thrombocytopenia ( < 50, 000/µL), coagulopathy
12)History of coronary artery disease or gastrointestinal (GI) bleeding
13)Post-anoxic coma; status epilepticus; Parkinson; central nervous system (CNS) infections (community-acquired; hospital-acquired; ventriculitis; post-operative)
14)Pregnancy or breastfeeding patient
15)Life expectancy less than 3 month
16)DNR (do not resuscitate) ordered patient

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Depression scale
Secondary Outcome Measures
NameTimeMethod
Cognitive impair scale;Neurologic deficit
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