Surgical reconstruction using the human dried amnion of the otolaryngology regio
- Conditions
- The patients with the mucosa defect of the otolaryngology region receiving surgical treatment
- Registration Number
- JPRN-UMIN000031097
- Lead Sponsor
- niversity of Toyama
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 150
Not provided
1) The person who judged a doctor to have difficulty in hospital visiting and coming home safely for study period 2) The patients who complicate infection with the activity 3) The patients who plan the enforcement of the operation for the evaluation department effective during study period in (perform a study of the agreement acquisition with starting) 4) For the group medicine of the planned drug (Xylocaine anesthetic agent, Achromycin) to use during study period, is the patients with a history of the drug allergy 5) The patients (saying that, however, the subjects who do not receive the study drug are possible) who participated in other studies or clinical studies within six months 6) Pregnancy or the childbearing patients who may be pregnant or hope for pregnancy during study period or do not use appropriate contraception 7) The patients who judged a doctor to be inadequate as an object of this study in testing at agreement acquisition
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Day to Epithelization completion after treatment (The epithelization completion defines "the point in time when the summation of each item score became 0" as "epithelization completion" at each evaluation point of "pain, otorrhea, adhesion, color, the neovascularisation".)
- Secondary Outcome Measures
Name Time Method 1)Pain 2)otorrhea 3)adhesion 4)color 5)neovascularisation