Unique ID issued by UMIN | UMIN000001123 |
---|---|
Receipt number | R000001371 |
Scientific Title | A phase II study of percutaneous radiofrequency ablation for malignant reanl tumor (JIVROSG-0701) |
Date of disclosure of the study information | 2008/04/22 |
Last modified on | 2012/03/10 18:56:12 |
A phase II study of percutaneous radiofrequency ablation for malignant reanl tumor (JIVROSG-0701)
Percutaneous radiofrequency ablation for malignant renal tumor (JIVROSG-0701)
A phase II study of percutaneous radiofrequency ablation for malignant reanl tumor (JIVROSG-0701)
Percutaneous radiofrequency ablation for malignant renal tumor (JIVROSG-0701)
Japan |
malignant renal tumor
Medicine in general | Cardiology | Endocrinology and Metabolism |
Hematology and clinical oncology | Nephrology | Surgery in general |
Vascular surgery | Endocrine surgery | Urology |
Radiology |
Malignancy
NO
To evaluate the safety and efficacy of percutaneous radiofrequency ablation for malignant renal tumor.
Safety,Efficacy
Confirmatory
Explanatory
Phase I,II
Adverse events
Response rate of tumor shrinkage on RECIST
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Maneuver |
A radiofrequency needle is inserted into the renal tumor percutaneously, and then, radiofrequency tumor ablation is performed.
Not applicable |
Not applicable |
Male and Female
1) Histologically or imaging confirmed malignant renal tumor.
2) Having at least one target lesion with maximum diameter on CT image between 1.0cm and 3.cm.
3) Target lesion shows the increase of HU more than 20 on CT by contrast enhacement.
4) Surgical treatment is out of indication or refused.
ous loco-regional therapy for the tumor.
5) Adequate cardiac, hepatic, renal, respiratory, coagulation, and bone marrow functions.
6) Age less than 20 at informed consent.
7) Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
8) Expected survival more than 2 months.
9) Written informed consent.
1) Cardiac pacemaker.
2) Artery, nerve or ureter exists on the puncture route.
3) Target lesion adjacent to renal pelvis, or a RFA needle can not be inserted without passing through renal pelvis or alimentary tract.
4) Non-mesurable target lesion on CT.
5) Colinically significant bleeding tendency or abnormal coagulation.
6) Tentative stop of anti-platelet or anti-coagulant medication is not allowed.
7) Drug allergy
8) With active infection
9) With active inflammation
10) Fever above 38 degrees Celsius.
11) If having multiple lesions, no treatment of tumors except a target lesion for 4 weeks after the treatment for a target lesion is not allowed.
12) Stop of chemotherapy or immunotherapy for 4 weeks after the treatment for a target lesion is not allowed.
13) Previous reginal therapy for the target lesion.
14) Pregnancy.
33
1st name | |
Middle name | |
Last name | Susumu Kanazawa |
Okayama University
Department of Radiology
2-5-1, Shikada-cho, Okayama, 700-8558, Japan
086-235-7313
1st name | |
Middle name | |
Last name | Yasuaki Arai |
JIVROSG, Coordinating Office
Division of Diagnostic Radiology, National Cancer Center Hospital
5-1-1, Tsukiji, Chu0-ku, Tokyo, 104-0045, Japan
03-3542-2511
http://jivrosg.umin.jp/
jivrosgoffice@ml.res.ncc.go.jp
Japan Interventional Radiology in Oncology Study Group (JIVROSG)
Ministry of Health, Labour and Welfare
Japan
NO
2008 | Year | 04 | Month | 22 | Day |
Unpublished
Completed
2008 | Year | 02 | Month | 29 | Day |
2008 | Year | 04 | Month | 01 | Day |
2010 | Year | 08 | Month | 01 | Day |
2010 | Year | 08 | Month | 01 | Day |
2010 | Year | 08 | Month | 01 | Day |
2010 | Year | 10 | Month | 01 | Day |
2008 | Year | 04 | Month | 21 | Day |
2012 | Year | 03 | Month | 10 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000001371