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

COMPLETED NA

Assessment of the Embolization of Neurovascular Lesions Using the Penumbra Smart Coil

NCT02729740 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to gather post market data on the Penumbra SMART COIL® System (Smart System) in the treatment of intracranial aneurysms and other malformations.

Conditions Studied

Interventions

  • DEVICE Penumbra Smart Coil
  • DEVICE Penumbra Coil 400TM (PC400), Penumbra Occlusion DeviceTM(POD)

Study Locations (20)

Florida

  • Lawnwood Regional Medical Center — Ft. Pierce
  • CARE - Palmetto — Hialeah
  • Memorial Healthcare System — Hollywood
  • Baptist Medical Center — Jacksonville
  • Mayo Clinic Jacksonville — Jacksonville
  • Jackson Memorial — Miami

Arizona

  • Banner Desert Medical Center — Mesa
  • Banner University Medical Center - Phoenix — Phoenix
  • BNI — Phoenix
  • Banner - University Medical Center Tucson — Tucson

California

  • Community Regional — Fresno
  • Loma Linda Medical Center — Loma Linda
  • Mercy San Juan — Sacramento
  • Cottage Hospital — Santa Barbara

Colorado

  • University of Colorado — Aurora
  • RIA - Swedish Medical Center — Englewood
  • St. Anthony's Hospital — Lakewood
  • RIA - Lutheran Medical Center — Wheat Ridge

Alabama

  • Southeast Alabama Medical Center — Dothan

Delaware

  • Christiana Health — Newark

Trial Details

FieldValue
Enrollment Target 995 participants
Start Date 2016-06-03
Est. Completion 2019-12-27
Phase NA

Sponsor

Penumbra

9 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02729740

The ClinicalTrials.gov registry entry for NCT02729740 describes a study currently listed as completed. 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 995 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Penumbra, which has 9 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 Intracranial Aneurysm appearing as the primary indexed condition, and to 2 interventions — of which Penumbra Smart Coil 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: NCT02729740 reports 20 study locations spanning 6 distinct geographic areas — top geographies include Florida, Arizona, California. 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 NCT02729740 about?

NCT02729740 is a clinical study titled "Assessment of the Embolization of Neurovascular Lesions Using the Penumbra Smart Coil". The primary objective of this study is to gather post market data on the Penumbra SMART COIL® System (Smart System) in the treatment of intracranial aneurysms and other malformations.

What is the current status of trial NCT02729740?

This trial is currently completed. It is a NA study. The enrollment target is 995 participants. The study started on 2016-06-03. Estimated completion is 2019-12-27.

What conditions does trial NCT02729740 study?

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

What interventions are being tested in trial NCT02729740?

The interventions under investigation include: Penumbra Smart Coil (DEVICE), Penumbra Coil 400TM (PC400), Penumbra Occlusion DeviceTM(POD) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02729740?

This trial is sponsored by Penumbra, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02729740 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Colorado, Delaware. 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