Clinical research for efficacy and safety of plastic surgery of the nose
Not Applicable
Completed
- Conditions
- Patient undergoing plastic surgery of the nose
- Registration Number
- JPRN-jRCT1090220220
- Lead Sponsor
- FUJI SOFT INCORPORATED, Department of Regenerative Medicine Research
- Brief Summary
It was confirmed that the appearance and QOL tended to improve, and that nasal height increase effect was maintained. It was also confirmed that no notable adverse events occurred.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 5
Inclusion Criteria
1. Patients with plans to repair the nose deformation by plastic surgery of the nose
2. Patients can agree to the shooting and provision of roentgenographic cephalogram
3. Patients more older than 17 years of age (at the time of obtaining informed consent)
4. Patients themselves and their representative (in the case of a patient is less than 20 years of age) can understand the contents of the investigation, and be able to get a written informed consent
Exclusion Criteria
1.Unsuitable patients as a target of investigation determined by medical doctor
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Patient background<br>2. Roentgenographic cephalogram<br>3. Adverse event
- Secondary Outcome Measures
Name Time Method 1. Research subjects questionnaire (DAS59, ADL, SDS)<br>2. Evaluation of autologous tissue (cartilage or bone) harvest site<br>3. Palpation<br>4. Standard facial photograph<br>5. head computerized tomography (CT)<br>6. head magnetic resonance imaging (MRI)