Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING NA

A Clinical Evaluation of the MicroSTent® PeripherAl Vascular SteNt in Subjects With Arterial Disease Below the Knee (STAND)

NCT03477604 · View on ClinicalTrials.gov ↗

Study Summary

Randomized multicenter clinical trial consisting of two arms; one arm treated with PTA plus the MicroStent® System and one arm treated with PTA alone. Purpose to evaluate the safety and effectiveness of using the MicroStent® Peripheral Vascular Stent System, hereafter referred to as the MicroStent® System, for the treatment of infrapopliteal lesions in subjects with peripheral arterial disease.

Interventions

  • DEVICE MicroStent and Standard PTA
  • DEVICE Standard PTA

Study Locations (20)

Florida

  • Palm Vascular — Fort Lauderdale
  • First Coast Cardiovascular Institute — Jacksonville
  • FHV Health — Leesburg
  • Mount Sinai Medical Center — Miami Beach
  • Advent Health Sebring — Sebring

New Jersey

  • Deborah Heart and Lung Center — Browns Mills
  • North Jersey Vascular Center — Clifton
  • AMI Vascular Institute — Galloway

Alabama

  • Cardiovascular Associates of the Southeast — Birmingham

Arizona

  • Copper State Vascular — Mesa

California

  • St. Helena Hospital — St. Helena

Colorado

  • Rocky Mountain Regional VA Medical Center — Aurora

Iowa

  • Vascular Institute of the Midwest — Davenport

Louisiana

  • Cardiovascular Institute of the South — Houma

Trial Details

FieldValue
Enrollment Target 177 participants
Start Date 2020-03-31
Est. Completion 2028-03
Phase NA

Sponsor

Micro Medical Solution

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03477604

The ClinicalTrials.gov registry entry for NCT03477604 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 177 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Micro Medical Solution, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Peripheral Arterial Disease appearing as the primary indexed condition, and to 2 interventions — of which MicroStent and Standard PTA is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03477604 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Florida, New Jersey, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03477604 about?

NCT03477604 is a clinical study titled "A Clinical Evaluation of the MicroSTent® PeripherAl Vascular SteNt in Subjects With Arterial Disease Below the Knee (STAND)". Randomized multicenter clinical trial consisting of two arms; one arm treated with PTA plus the MicroStent® System and one arm treated with PTA alone. Purpose to evaluate the safety and effectiveness of using the MicroStent® Peripheral Vascular Stent System, hereafter referred to as the MicroStent® ...

What is the current status of trial NCT03477604?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 177 participants. The study started on 2020-03-31. Estimated completion is 2028-03.

What conditions does trial NCT03477604 study?

This clinical trial studies the following conditions: Peripheral Arterial Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03477604?

The interventions under investigation include: MicroStent and Standard PTA (DEVICE), Standard PTA (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03477604?

This trial is sponsored by Micro Medical Solution, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03477604 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Colorado, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial