Planned reconstruction patients using microsurgery for congenital disease,trauma or tumor resections free flap transplantation thrombosis microsurgery
Conditions
Interventions
Application of device for 8days after surgery
Sponsors
Tomioka Yoko
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Patients who will have cosmetic/functional reconstruction surgery 2.Patients 18 years or older 3.Patients who have been informed about the study, and have agreed with it in written format.
Exclusion criteria
Exclusion criteria: 1.Pregnant woman 2.Nursing mothers 3.Observed infectious signs around the site for device installation 4.Patients who are not capable to corporate to this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation of Physician's findings and multipoint tissue circukation monitoring v2.0 | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Matching rate of patient prognosis and judgment by multipoint tissue circulation monitoring v2.0 2.Matching rate of Physician's findings and patient prognosis 3.Survey for usability 4.Adverse response and device failure | — |
Contacts
Public ContactYukiko Tahara
The University of Tokyo Hospital
Outcome results
None listed