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Examination about the curative effect of Mirtazapine for the QOL of the pulmonary tumor patient.

Examination about the curative effect of Mirtazapine for the QOL of the pulmonary tumor patient. - Examination about the curative effect of Mirtazapine for the QOL of the pulmonary tumor patient.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000024726
Enrollment
60
Registered
2017-04-01
Start date
2017-04-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Lung cancer and suspected case

Interventions

We carry out HADS (Hospital Anxiety and Depression Scale) to a patient of the lung cancer doubt, and having depressive symptom or not is screened. We give mirtazapine 15mg(after 14 days, up to 30mg) t

Sponsors

Kyoto Prefectural University of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patient who received written enough explanation about a purpose, a method, the significance of this study with a document agreement.

Exclusion criteria

Exclusion criteria: The patient who could not carry out HADS or was refused. The patient who has a history of the past with hypersensitivity for mirtazapine. The patient with a history of the past with brain disorder (including dementia and Parkinson's disease) of the tissue except the metastasis to brain. The patient with the past of Mental disease medicine treatment except the sleep inducing drug within three months. The patient with severe hepatic dysfunction or renal dysfunction. The patients with the past of suicide consideration or suicide project. The patients who receive medical treatment with heart trouble (myocardial infarction, angina, conduction disorder). The patient with glaucoma or the intraocular pressure sthenia. The patients who receive medical treatment with dysuria. During a pregnant woman, the nursing and the patient who may be pregnant. The patient who takes a monoamine oxidase inhibitor (MAOI) within two weeks. The patient who judged that the examination medical attendant was inappropriate.

Design outcomes

Primary

MeasureTime frame
Change of the total Hospital Anxiety and Depression Scale (HADS) score before and after 4 weeks treatment with mirtazapine.

Secondary

MeasureTime frame
Quick Inventory of Depressive Symptomatology (QIDS-J),Clinical Global Impression of Improvement (CGI).The change of the total HADS score during the observation period in the non-group given mirtazapine. A comparison of HADS in a mirtazapine treatment group and the non-treatment group.

Countries

Japan

Contacts

Public ContactYoshiko Kaneko

Kyoto Prefectural University of Medicine Pulmonary Medicine

kaneko-y@koto.kpu-m.ac.jp075-251-5513

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026