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Not yet recruitingNCT07628101PediasorbUpdated Jun 4, 2026

First-in-human Clinical Trial to Assess Safety and Efficacy of the CardiaZn Bioresorbable Stent in Children With Pulmonary Artery Stenosis and Aortic Coarctation

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

Phase
Not applicable
Study type
Interventional
Enrollment
45
Allocation
Not applicable
Ages
Up to 8 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Aortic Coarctation, Pulmonary Artery Stenosis

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Keywords

  • Bioresorbable stent
  • Pediatric stent
  • Aortic coarctation
  • Pulmonary artery stenosis
  • CardiaZn
  • PediaStent
  • PEDIASORB
  • biodegradable
03

In context

Aortic Coarctation

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 →

Lead sponsor

This is the only study on the registry with PediaStent LLC as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 8 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Subject is aged less than 9 years at the time of the index procedure
  • Subject presents with hemodynamically significant discrete aortic coarctation or pulmonary artery stenosis requiring catheter-based intervention
  • Subject meets angiographic eligibility criteria at the time of the index procedure as assessed by the interventional cardiologist
  • Subject's legally authorized representative has provided written prior to any study-related procedures
  • Subject's physician has determined that catheter-based intervention is clinically indicated
  • Target vessel anatomy is suitable for stent implantation as assessed by the operator

Exclusion criteria

Exclusion Criteria:

  • Subject has complex aortic arch hypoplasia or long segment coarctation not amenable to stent therapy
  • Subject has a known allergy or to zinc or silver
  • Subject has active systemic infection at the time of the index procedure
  • Subject has a to cardiac catheterization or general anesthesia
  • Subject has previously received a stent at the target vessel segment
  • Subject has a comorbid condition that in the opinion of the investigator would preclude safe participation in the study or confound study results
  • Subject is currently enrolled in another device or drug study that has not completed its primary endpoint
  • Subject has a of less than 12 months in the opinion of the investigator
Terms in these criteria, in plain language(5)

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.

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.

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.

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.

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.

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.

05

Study design

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

Study arms

  • Experimental
    CardiaZn Bioresorbable Stent

    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

Interventions

  • DeviceCardiaZn 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.

06

What researchers measure

Primary outcomes

  1. 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)

  2. 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

Secondary outcomes

  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. All-Cause Mortality

    Death from any cause

    Time frame: 30 days, 6 months, 12 months, annually through 5 years

  8. 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

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07628101
Lead sponsor
PediaStent LLC
Responsible party
Sponsor
First posted
Jun 4, 2026
Start date
Oct 2026 (estimated)
Primary completion
Oct 2031 (estimated)
Completion
Dec 2031 (estimated)
Last update
Jun 4, 2026

Study contacts

Timothy Moran President
Contact
trm242@gmail.com
8886916161
Daniel Levi, MD
study director · University of California, Los Angeles

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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