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NCT07240259Enrolling by invitation

Feasibility of Tracheobronchial Reconstruction Using Allogenic Aortic Patch in Children

Source: ClinicalTrials.gov · Last updated 17 Aug 2026

Brief summary (registry, in English)

Feasibility and safety of repairing tracheal and bronchial defects in infants and children using cryopreserved donor aortic patches.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
5 (estimated)
First submitted
12 Sept 2025
Start date
1 Dec 2026
Primary completion date
31 Jan 2028
Lead sponsor
National Taiwan University Hospital
Diseases
Tuberculosis
NCT number
NCT07240259

What you commit to

  • Study type: Interventional
  • Planned participants: 5
  • From 1 Dec 2026 to the primary completion date, 31 Jan 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Malignant solid tumors with distant metastases that cannot be completely resected surgically or controlled with medication.
  • Presence of severe immunodeficiency (e.g., congenital immunodeficiency, HIV infection, ongoing chemotherapy, or recovery period after bone marrow transplantation).
  • Presence of major congenital diseases or chromosomal abnormalities (e.g., Trisomy 13, Trisomy 18) with extremely poor prognosis as assessed clinically.
  • End-stage organ failure (e.g., persistent multiple organ failure, irreversible cardiopulmonary failure, or brain death).

Other

  • Inability to obtain legal informed consent from the lawful guardian.
  • Locally invasive tracheal tumors that cannot be completely resected surgically.

Who the study is looking for

  • Meeting any of the following conditions, and being unsuitable for standard end-to-end tracheal anastomosis or lacking sufficient native tracheal tissue for defect reconstruction:
  • Congenital tracheal malformations: including congenital tracheomalacia, congenital tracheobronchial anomalies, complete tracheal rings, etc., with severe clinical respiratory symptoms and recommended for treatment after evaluation.
  • Acquired tracheal stenosis: including tracheal narrowing caused by disease, endotracheal intubation, or postoperative scar formation, with severe clinical respiratory symptoms and recommended for treatment after evaluation.
  • Tracheal injury or tissue loss due to trauma or burns requiring surgical repair.
  • Tracheal tumors: reconstruction of tracheal tissue after resection of benign or malignant tumors.
  • The term "severe clinical respiratory symptoms" includes:
    • Dependence on mechanical ventilation for more than 1 month due to airway narrowing or defect, with inability to wean.
    • Airway stenosis exceeding 50% (confirmed by bronchoscopy or CT imaging), accompanied by persistent stridor, inspiratory dyspnea, or suprasternal/substernal retractions, causing impairment of daily activities or feeding difficulties.
    • Unilateral or bilateral lung atelectasis persisting for more than 1 month due to tracheal or bronchial stenosis, with no sign of recovery.
    • Recurrent post-obstructive pneumonia (≥3 episodes) in one or both lungs caused by tracheal or bronchial stenosis, requiring hospitalization for treatment.

Age in the registry: 0 years to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Taiwan National Taiwan University Hospital
Coordinator of this site? Confirm its status
TaipeiTaiwanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.