Unique ID issued by UMIN | UMIN000039147 |
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Receipt number | R000044647 |
Scientific Title | A multicenter prospective observational study on the structured parenteral opioid intervention for dyspnea in terminally-ill cancer patients |
Date of disclosure of the study information | 2020/01/20 |
Last modified on | 2022/01/16 08:45:56 |
A multicenter prospective observational study on the structured parenteral opioid intervention for dyspnea in terminally-ill cancer patients
A multicenter prospective observational study on the structured parenteral opioid intervention for dyspnea in terminally-ill cancer patients
A multicenter prospective observational study on the structured parenteral opioid intervention for dyspnea in terminally-ill cancer patients
A multicenter prospective observational study on the structured parenteral opioid intervention for dyspnea in terminally-ill cancer patients
Japan |
Advanced cancer
Hematology and clinical oncology |
Malignancy
NO
To describe the practice of a structured parenteral opioid intervention for dyspnea in terminally-ill cancer patients
Others
To explore outcomes of a structured parenteral opioid intervention for dyspnea in terminally-ill cancer patients.
Exploratory
The percentage of patients who receive a structured parenteral opioid intervention at 24 (18-30) hours after the initiation of the intervention for dyspnea
The percentage of the utilization of a structured parenteral opioid intervention, achievement of treatment goals, contents of concurrent treatment such as increase and/or switching of opioids and benzodiazepines, dyspnea intensity, communication capacity and consciousness level, adverse events and dose-limiting toxicities, etc.
Observational
18 | years-old | <= |
Not applicable |
Male and Female
1) Hospitalized patients with the age of 18 or greater
2) Patients diagnosed with locally advanced or metastatic cancer
3) Patients started on the continuous administration of parenteral opioids for dyspnea (IPOS/STAS of 2 or greater)
4) Patients receiving care by palliative care specialist(s) at a palliative care unit or palliative care team
5) ECOG Performance Status 3 or 4
6) Communication Capacity Scale (CCS), item 4 of 2 or lower
1) Patients who will receive treatent for dyspnea that clearly has no direct pathophysiological association with cancer
2) Patients who are planning to undergo interventions that would change symptom intensity during a short period within 3 days.
3) Patient or family decline to participation
100
1st name | Masanori |
Middle name | |
Last name | Mori |
Seirei Mikatahara General Hospital
Palliative and Supportive Care Division
433-8558
3453 Mikataharacho, Kita-ku, Hamamatsu
0534361251
masanori.mori@sis.seirei.or.jp
1st name | Masanori |
Middle name | |
Last name | Mori |
Seirei Mikatahara General Hospital
Palliative and Supportive Care Division
433-8558
3453 Mikataharacho, Kita-ku, Hamamatsu
0534361251
masanori.mori@sis.seirei.or.jp
Seirei Mikatahara General Hospital
Ministry of Health, Labour, and Welfare
Japan Hospice Palliative Care Foundation
Japanese Governmental office
Seirei Mikatahara General Hospital
3453 Mikataharacho, Kita-ku, Hamamatsu
0534361251
masanori.mori@sis.seirei.or.jp
NO
2020 | Year | 01 | Month | 20 | Day |
Unpublished
No longer recruiting
2019 | Year | 12 | Month | 30 | Day |
2020 | Year | 01 | Month | 20 | Day |
2020 | Year | 01 | Month | 20 | Day |
2021 | Year | 06 | Month | 30 | Day |
2021 | Year | 10 | Month | 31 | Day |
Seirei Mikatahara General Hospital serves as the central site of this multicenter study.
2020 | Year | 01 | Month | 14 | Day |
2022 | Year | 01 | Month | 16 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000044647
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