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

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

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
CRIS
Registry ID
KCT0005453
Enrollment
112
Registered
2020-10-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : Study Design This is a prospective, randomized, multi-center study conducted in different Korean intensive care units (ICUs). This objective of the study is to evaluate the incidence of major d

Sponsors

Asan Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Depression scale

Secondary

MeasureTime frame
Cognitive impair scale;Neurologic deficit

Countries

Korea, Republic of

Contacts

Public ContactMoinay Kim

University of Ulsan

aussie84@naver.com+82-2-3010-3550

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026