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A multicenter clinical study of functional tracheal remodeling with an artificial trachea

Not Applicable
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
Inclusion Criteria

Not provided

Exclusion Criteria

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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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