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WithdrawnNCT03405636Updated Apr 9, 2021

Xeltis Pulmonary Valved Conduit Safety and Performance Study

An interventional study of Xeltis Pulmonary Valved Conduit in Heart Defects, Congenital, sponsored by Xeltis. Withdrawn at 4 sites in 4 countries. Open to participants aged Up to 21 Years. Per ClinicalTrials.gov, last updated 2021-04-09.

Sponsored by Xeltis · Not applicable, Interventional, and Treatment

Why this study was withdrawn
Study not started
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
Up to 21 Years
Sex
All
01

Study summary

This is a multi-center prospective, single-arm, non-randomized, open label study to assess safety and performance of the Xeltis Pulmonary Valved Conduit in subjects requiring Right Ventricular Outflow Tract correction or reconstruction due to congenital heart malformations.

02

Conditions studied

  • Heart Defects, Congenital
03

Who can participate

Ages eligible
Up to 21 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Patient requiring RVOT reconstruction, suitable for 16 mm or 18 mm valved conduit.
  2. Male or Female.
  3. Age \< 22 years.
  4. Right Ventricular to Pulmonary Artery mean gradient > 35mm Hg or moderate or severe Pulmonary regurgitation (≥3+), or have both.
  5. The patient, and the patient's parent / legal representative where appropriate, has been informed of the nature of the study, agrees to its provisions and has provided written informed consent by signing the approved informed consent form.
  6. The patient, and the patient's parent / legal representative where appropriate, and the treating physician agree that the subject will return for all required post-procedure follow up visits and the subject will comply with clinical investigation plan required follow-up visits.

Exclusion criteria

Exclusion Criteria:

  1. Need for or presence of prosthetic heart valve at other position
  2. Need for concomitant surgical procedures (non-cardiac)
  3. Patients with previously implanted pacemaker (including defibrillators) or mechanical valves
  4. Active bacterial or viral infection or requiring current antibiotic therapy (if temporary illness, patient may be a candidate 4 weeks after discontinuation of antibiotics)
  5. Active endocarditis
  6. Leukopenia, according to local laboratory evaluation of white blood cell count
  7. Acute or chronic anemia, according to local laboratory evaluation of hemoglobin Patients can be transfused to meet eligibility criteria
  8. Thrombocytopenia, defined as Platelet count \< 150,000/mm3 Patients can be transfused to meet eligibility criteria
  9. Severe chest wall deformity, which would preclude placement of the PV conduit
  10. Pulmonary hypertension (right ventricular systolic pressure ≥ half of systemic systolic pressure)
  11. Right ventricular outflow tract aneurysm
  12. Known hypersensitivity to anticoagulants and antiplatelet drugs and to the device materials
  13. Immunocompromised patient defined as: autoimmune disease, patients receiving immunosuppressant drugs or immune stimulant drugs
  14. Patient has chronic inflammatory / autoimmune disease
  15. Need for emergency cardiac or vascular surgery or intervention
  16. Major or progressive non-cardiac disease (liver failure, renal failure, cancer) that has a life expectancy of less than one year
  17. Currently participating, or participated within the last 30 days, in an investigational drug or device study
  18. Alcohol or drug abuse as defined by DSM IV-TR criteria for substance abuse - this includes the illicit use of cannabis within the last 12 months
  19. Females who are sexually active and are not willing to use adequate contraceptive precautions for the next 2 years
  20. Patient has medical, social or psychosocial factors that, in the opinion of the Investigator, could have impact on safety or compliance
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Xeltis Pulmonary Valved Conduit

    PV Conduit for RVOT reconstruction

    Device: Xeltis Pulmonary Valved Conduit

Interventions

  • DeviceXeltis Pulmonary Valved Conduit

    RVOT reconstruction

05

What researchers measure

Primary outcomes

  1. Survival at 12 months follow up post implantation

    Measured by the fact that the patient is still alive at the time of the 12 month FU visit

    Time frame: 12 months

Secondary outcomes

  1. Freedom from device related death, intervention and/or reoperation at 12 months follow up

    Measured by the fact that the patient did not die, did not have a reoperation or reintervention during the first 12 months

    Time frame: 12 months

  2. Mean pressure gradient across the area of conduit implantation (RV to PA) of less than 40 mm Hg at 12 months follow up

    Time frame: 12 months

  3. Pulmonary regurgitation of equal or less than moderate (≤40 %) at 12 months follow up

    Time frame: 12 months

06

Study locations

4 sites
  • Gottsegen György Hungarian Institute of Cardiology, Paediatric Cardiac Centre
    Budapest, H-1096, Hungary
  • Institute Jantung Negara, National Heart Institute
    Kuala Lumpur, Malaysia
  • University Children's Hospital of Cracow (UCH),
    Krakow, 30-663, Poland
  • Childrens Heart Centre Slovak Republic
    Bratislava, Slovakia
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03405636
Lead sponsor
Xeltis
Responsible party
Sponsor
First posted
Jan 23, 2018
Start date
Sep 2020 (estimated)
Primary completion
Oct 2021 (estimated)
Completion
Oct 2026 (estimated)
Last update
Apr 9, 2021

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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