RecruitingPhase 2NCT04467671

Two-Year Study of the Safety and Efficacy of the Second-Generation Tissue Engineered Vascular Grafts

Prospective, Open-labeled, Single-arm Clinical Trial to Evaluate the Safety and Efficacy of the Second-generation Tissue Engineered Vascular Graft as Vascular Conduits for Extracardiac Total Cavopulmonary Connection.


Sponsor

Nationwide Children's Hospital

Enrollment

24 participants

Start Date

Jul 15, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

A single arm clinical trial evaluating the safety and efficacy of the second generation TEVG as vascular conduits for extracardiac total cavopulmonary connection.


Eligibility

Inclusion Criteria3

  • Patients will be eligible for inclusion in the study if they meet all of the following criteria.
  • Patient must be a candidate to undergo an extracardiac total cavopulmonary connection.
  • Patient and/or legal guardian must voluntarily provide informed consent/assent for participation in the study.

Exclusion Criteria12

  • Patients will be excluded from participation in the study if they meet any of the following criteria.
  • Patient has an urgent/emergent operative status.
  • Patient has acute renal failure or renal insufficiency in the opinion of the investigator
  • Patient requires a graft less than 12 mm or greater than 24 mm in diameter.
  • Patient has a pacemaker.
  • Patient has pulmonary vascular resistance greater than 4 um2 (u=Wood's units)
  • Patient has abnormal venous drainage (interrupted inferior vena cava \[IVC\]).
  • Patient presents with significant atrio-ventricular valve regurgitation that in the opinion of the investigator, makes them ineligible.
  • Patient has a history of another condition or significant medical problem that, in the opinion of the investigator, precludes compliance with protocol-specified procedures.
  • Patients taking any medications that in the opinion of the Investigator could interfere with the TEVG, including bisphosphonates (i.e. Clodronate or Zoledronate).
  • Patient or parent/legal guardian is, in the opinion of the investigator, unable to comply with protocol evaluations.
  • Preoperative hemoglobin \<11.0 mg/dL at time of patient's pre-admission testing.

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Interventions

COMBINATION_PRODUCTTissue Engineered Vascular Grafts

Patients will undergo EC TCPC interposition grafting with a tissue engineered vascular graft and serial magnetic resonance imaging (MRI)


Locations(1)

Nationwide Children's Hospital

Columbus, Ohio, United States

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NCT04467671