Skip to content

Effectiveness verification of Mirtazapine Patients with Acute Anxiety

Effectiveness verification of Mirtazapine in Patients with Acute Anxiety

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CRIS
Registry ID
KCT0008183
Enrollment
52
Registered
2023-02-14
Start date
2023-01-17
Completion date
Unknown
Last updated
2023-05-02

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

Conditions

None listed

Interventions

Drug : Patients diagnosed with major depressive disorder are recruited from the outpatient department of psychiatry at Chung-Ang University Hospital. Patients with major depressive disorder with acute

Sponsors

Chung-Ang Univerisity Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? The age of 18 to 65 ? A person diagnosed as a major depressive disorder without psychotic features. by Structured Clinical Interview for DSM-5 (SCID-5) ? BAI scale score is 16 or higher (with moderate or higher anxiety symptoms) ? Those who have no history of using Mirtazapine in the last two months based on the initial evaluation point ? Those who have been administering antidepressants (SSRI, SNRI and NDRI) at stable doses for more than 1 month

Exclusion criteria

Exclusion criteria: ? A person who has been diagnosed other psychiatric diagnosis by SCID-5-CV in the past ? Those who currently have severe medical conditions (cancer, heart failure, kidney failure, liver disease, lung disease, thyroid disease and acute inflammatory conditions) ? A person who has a history of past or present dependence on substances or misuse ? A person with a history of epilepsy, head trauma, and organic mental illness

Design outcomes

Primary

MeasureTime frame
mean change of Beck anxiety inventory (BAI) scores from baseline

Secondary

MeasureTime frame
mean change of Beck depressive inventory (BDI-II) scores from baseline;mean change of Korean Symptom Check List 95 (KSCL95) scores from baseline;mean change of CGI-S scores from baseline;CGI-I scores after 8 weeks of intervention;hemodynamic changes in prefrontal cortex measured with functional Near-Infrared Spectroscopy(fNIRS)

Countries

Korea, Republic of

Contacts

Public ContactHee Jin KIM

Chung-Ang Univerisity Hospital

iamheejin2@cauhs.or.kr+82-2-6299-1508

Outcome results

None listed

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