Unique ID issued by UMIN | UMIN000018054 |
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Receipt number | R000020906 |
Scientific Title | Prospective study of efficacy of negative pressure wound therapy for surgical site infection after hepatobiliary and pancreatic surgery |
Date of disclosure of the study information | 2015/06/25 |
Last modified on | 2017/06/27 00:14:04 |
Prospective study of efficacy of negative pressure wound therapy for surgical site infection after hepatobiliary and pancreatic surgery
Prospective study of efficacy of negative pressure wound therapy for surgical site infection after hepatobiliary and pancreatic surgery
Prospective study of efficacy of negative pressure wound therapy for surgical site infection after hepatobiliary and pancreatic surgery
Prospective study of efficacy of negative pressure wound therapy for surgical site infection after hepatobiliary and pancreatic surgery
Japan |
Surgical site infection
Surgery in general | Hepato-biliary-pancreatic surgery |
Others
NO
The aim of this study is to evaluate the efficacy of negative pressure wound therapy for surgical site infection after hepatobiliary and pancreatic surgery
Efficacy
The duration from incidence of surgical site infection to wound healing
The postoperative hospital stay, the cost of hospitalization, the presence of reopened wound, the presence and degree of adverse events
Interventional
Single arm
Non-randomized
Open -no one is blinded
Historical
1
Treatment
Device,equipment |
For the patients with surgical site infection after hepatobiliary and pancreatic surgery, unroofing and debridement of infected wound is performed. Therefore, negative pressure wound therapy is started and continued for 1-2 weeks. After recognizing a formation of wound granulation, the wound is closed by suture.
20 | years-old | <= |
Not applicable |
Male and Female
1, The patients with surgical site infection after hepatobiliary and pancreatic surgery
2, Older than 20 years old
3, ECOG performance status of 0 to 2
4, Estimated survival is over 6 months
5, Documented informed consent
1, Naked blood vessel suspected of bleeding or surgical site infection to directly contact to other organs or the presence of fistula to abdominal cavity.
2, The presence of organ/space surgical site infection
3, As determined by the principal investigator or the sub-investigator the subject is not adequate to participate in the study.
70
1st name | |
Middle name | |
Last name | Hidetoshi Eguchi |
Osaka University, Graduate School of Medicine
Department of Gastroenterological Surgery
2-2 Yamadaoka, Suita, Osaka, Japan
+81-6-6879-3251
heguchi@gesurg.med.osaka-u.ac.jp
1st name | |
Middle name | |
Last name | Takehiro Noda |
Osaka University, Graduate School of Medicine
Department of Gastroenterological Surgery
2-2 Yamadaoka, Suita, Osaka, Japan
+81-6-6879-3251
tnoda@gesurg.med.osaka-u.ac.jp
Multicenter Clinical Study Group of Osaka
Osaka University, Graduate School of Medicine
Department of Gastroenterological Surgery
Self funding
NO
2015 | Year | 06 | Month | 25 | Day |
Unpublished
Open public recruiting
2015 | Year | 06 | Month | 11 | Day |
2015 | Year | 06 | Month | 11 | Day |
2015 | Year | 06 | Month | 24 | Day |
2017 | Year | 06 | Month | 27 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020906
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