A multicenter clinical study of functional tracheal remodeling with an artificial trachea
- Conditions
- Malignancies, inflammatory diseases, traumas
- Registration Number
- JPRN-UMIN000026634
- Lead Sponsor
- Kyoto University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 5
Not provided
Have a bilateral vocal fold palsy. Have a severe cardiovascular, hematological, hepatic, digestive, renal, pulmonary, endocrine, neurological or psychiatric diseases. Severe hemorrhage or shock. Severe bacterial, viral or fungal infections. Keloid diathesis. A history of irradiation to the neck. Be indicated for any other treatments. Have a history of allergic reaction to a porcine collagen or polypropylene. Have participated in any other clinical trials, and an investigational agent has been administered within 12 weeks. Pregnant, lactating, or willing to be pregnant during the trial. Be concluded not eligible to enter the trial by a principle investigator or sub-investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method