An interventional study of CardiaZn Bioresorbable Stent in Aortic Coarctation, Pulmonary Artery Stenosis, sponsored by PediaStent LLC. Not yet recruiting. Open to participants aged Up to 8 Years. Per ClinicalTrials.gov, last updated 2026-06-04.
Sponsored by PediaStent LLC · Not applicable, Interventional, and Treatment
This study evaluates the safety and effectiveness of the CardiaZn stent, a novel bioresorbable stent designed specifically for infants and children with congenital cardiovascular conditions. Unlike permanent metal stents, the CardiaZn stent is designed to open narrowed blood vessels and then gradually dissolve, leaving nothing permanently behind. This allows the vessel to grow naturally with the child over time.
The study will enroll children under 9 years of age diagnosed with either pulmonary artery stenosis - a narrowing of the arteries that carry blood from the heart to the lungs - or aortic coarctation - a narrowing of the main artery carrying blood from the heart to the body. Both conditions currently require repeated interventions as children grow, since existing permanent stents cannot accommodate natural vessel growth.
Participants will receive the CardiaZn stent during a standard cardiac catheterization procedure and will be followed for 5 years to assess vessel patency, device performance, and long-term safety outcomes.
Background and Clinical Need Pulmonary artery stenosis (PAS) and aortic coarctation (CoA) are among the most common congenital cardiovascular conditions requiring catheter-based intervention in infants and children. Current standard of care involves balloon dilation and implantation of permanent metallic stents. While effective in the short term, permanent stents present a significant limitation in pediatric patients: they cannot accommodate somatic growth, necessitating repeated balloon dilations and re-interventions throughout childhood. Furthermore, permanent metallic implants preclude normal vessel remodeling, restrict MRI imaging quality, and complicate future surgical access.
The unmet clinical need is substantial. A bioresorbable stent that provides acute vessel support, maintains patency through the critical healing phase, and then completely resorbs - leaving no permanent implant - would represent a paradigm shift in the management of pediatric congenital cardiovascular stenoses.
Device Description The CardiaZn stent is a bioresorbable endovascular stent fabricated from a zinc-silver (ZnAg) alloy. Zinc is an essential trace element with well-characterized metabolic pathways, and its corrosion byproducts are biocompatible and cleared through normal physiological mechanisms. The addition of silver enhances mechanical properties including radial strength and corrosion kinetics. The device is balloon-expandable and delivered via standard cardiac catheterization technique.
The ZnAg alloy platform distinguishes CardiaZn from polymer-based bioresorbable scaffolds, which have demonstrated limitations in radial strength and degradation kinetics, and from magnesium-based platforms, which resorb too rapidly for the intended application window. The zinc-silver system is designed to provide sufficient radial support through the vessel healing phase, with a resorption timeline aligned to the biological requirements of pediatric vascular remodeling.
The device is drug-free, relying entirely on the mechanical and biological properties of the ZnAg alloy to achieve its clinical objectives. This drug-free positioning is supported by pediatric case data from magnesium-based platforms demonstrating that bioresorbable metal scaffolds can achieve clinically meaningful outcomes without pharmacological augmentation.
Study Rationale Preclinical evaluation of the CardiaZn stent has included comprehensive in vitro testing, biocompatibility assessment per ISO 10993 standards, and a GLP animal study. Results have demonstrated adequate radial strength, biocompatible corrosion byproduct profile, and vessel patency consistent with the intended clinical application. These data support proceeding to first-in-human evaluation under an FDA Investigational Device Exemption.
Prior FDA engagement through the TAP Pre-Submission program (Q-Submission U230126-A010) established alignment on study design, endpoint selection, and statistical approach prior to IDE submission.
Study Design PEDIASORB is a prospective, multicenter, single-arm, open-label, pivotal clinical study. A total of 45 eligible subjects will be enrolled at up to 11 investigational sites. The study population includes subjects aged under 9 years presenting with hemodynamically significant discrete aortic coarctation or pulmonary artery stenosis.
To ensure balanced representation of both indications, neither the pulmonary artery stenosis nor the aortic coarctation population may contribute more than 70% of total enrollment, ensuring a minimum of 14 subjects per treatment location. At least 50% of enrollments will occur at United States investigational sites.
Patients will be screened for pre-operative eligibility within 60 days prior to the index procedure. Following confirmation of intraoperative eligibility criteria via angiography, eligible subjects will undergo implantation of the CardiaZn stent via standard cardiac catheterization technique.
Follow-Up All subjects will be followed for 5 years post-procedure. Follow-up visits are scheduled at hospital discharge and at months 1, 3, 6, and 12, and annually through year 5. Each follow-up visit includes physical examination, laboratory testing, health status assessment, imaging evaluation, and review of concomitant medications and procedures. CT angiography will be performed in all subjects at 6 months post-procedure.
Adverse events will be collected from initial informed consent through study exit.
Primary Endpoints
The co-primary endpoints are:
Device success at the index procedure, defined as successful delivery and deployment of the CardiaZn stent with achievement of adequate vessel patency as assessed by angiography Freedom from pre-defined procedure- and device-related serious adverse events of interest through 6 months post-procedure
Secondary Endpoints Secondary endpoints include assessment of vessel patency, peak-to-peak pressure gradient, vessel diameter, and freedom from re-intervention through 5 years of follow-up. Long-term safety will be assessed through collection of all adverse events, serious adverse events, and device-related complications through study exit.
Statistical Considerations The study is designed as a single-arm pivotal trial with performance goal comparisons against pre-specified objective performance criteria derived from published literature and historical data for the current standard of care. The sample size of 45 subjects provides adequate statistical power to test the co-primary endpoints at the pre-specified significance level. A formal statistical analysis plan has been developed and is included as an attachment to the IDE submission.
Data Safety Monitoring An independent Data Safety Monitoring Board (DSMB) will provide ongoing oversight of subject safety throughout the trial. A Clinical Events Committee (CEC) will provide independent adjudication of all adverse events and endpoints. Interim analyses will be conducted per the DSMB charter.
Regulatory Background The CardiaZn stent is an investigational device. This study is being conducted under FDA IDE number U230126. Prior FDA engagement was conducted through the TAP Pre-Submission program. The study is sponsored by PediaStent and conducted in accordance with applicable FDA regulations, Good Clinical Practice guidelines, and the principles of the Declaration of Helsinki.
49 studies on the registry are indexed under Aortic Coarctation; 16 are open to participants now.
This study's planned enrollment of 45 is close to the median of 45 across 19 interventional studies indexed under Aortic Coarctation.
Browse Aortic Coarctation studies →This is the only study on the registry with PediaStent LLC as lead sponsor.
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Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hypersensitivity
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Contraindication
A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Investigational drug or device
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Life expectancy
The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
All enrolled subjects will receive the CardiaZn bioresorbable zinc-silver alloy stent, delivered via standard cardiac catheterization technique for the treatment of hemodynamically significant aortic coarctation or pulmonary artery stenosis in subjects aged under 9 years.
Device: CardiaZn Bioresorbable Stent
The CardiaZn stent is a balloon-expandable bioresorbable endovascular stent fabricated from a zinc-silver (ZnAg) alloy. Zinc is an essential trace element with well-characterized metabolic pathways and biocompatible corrosion byproduct profile. The addition of silver enhances radial strength and optimizes corrosion kinetics for the intended resorption timeline. The device is delivered via standard cardiac catheterization technique under fluoroscopic guidance and is designed to provide acute mechanical support of the stenotic vessel segment following balloon dilation, then gradually resorb completely over time leaving no permanent implant. The device is drug-free.
Device Success at Index Procedure
Successful delivery and deployment of the CardiaZn stent with achievement of adequate vessel patency defined as less than 30% residual diameter stenosis as assessed by quantitative angiography
Time frame: At index procedure (Day 0)
Freedom from Device- and Procedure-Related Serious Adverse Events
Freedom from pre-defined procedure- and device-related serious adverse events of interest including vessel perforation, stent thrombosis, stent embolization, stent fracture, and target vessel reintervention
Time frame: 6 months post-procedure
Peak-to-Peak Pressure Gradient
Change in peak-to-peak pressure gradient across the treated vessel segment as measured by cardiac catheterization
Time frame: Baseline, 6 months, 12 months, annually through 5 years
Minimum Lumen Diameter
Minimum lumen diameter of the treated vessel segment as assessed by quantitative angiography or CT angiography
Time frame: Baseline, 6 months, 12 months, annually through 5 years
Freedom from Target Vessel Reintervention
Freedom from any reintervention at the target vessel segment including repeat balloon dilation, repeat stenting, or surgical intervention
Time frame: 6 months, 12 months, annually through 5 years
Freedom from Device- and Procedure-Related Serious Adverse Events
Freedom from pre-defined procedure- and device-related serious adverse events of interest
Time frame: 12 months, annually through 5 years
Stent Patency
Binary assessment of stent patency defined as absence of significant in-stent restenosis greater than 50% diameter stenosis as assessed by CT angiography or cardiac catheterization
Time frame: 6 months, 12 months, annually through 5 years
Somatic Growth Accommodation
Assessment of vessel diameter growth relative to somatic growth parameters including height and weight over the follow-up period
Time frame: 12 months, annually through 5 years
All-Cause Mortality
Death from any cause
Time frame: 30 days, 6 months, 12 months, annually through 5 years
Device-Related Adverse Events
All adverse events adjudicated as device-related by the independent Clinical Events Committee
Time frame: From index procedure through 5 years
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Plan to share: No
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