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Completed Not applicable Interventional Results available

Evaluating the Safety and Efficacy of the Indigo® Aspiration System in Acute Pulmonary Embolism

ClinicalTrials.gov ID: NCT03218566

Public ClinicalTrials.gov record NCT03218566. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 11:59 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Multicenter Trial to Evaluate the Safety and Efficacy of the Indigo® Aspiration System in Acute Pulmonary Embolism

Study identification

NCT ID
NCT03218566
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Penumbra Inc.
Industry
Enrollment
119 participants

Conditions and interventions

Interventions

  • Indigo Aspiration System Device

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 21, 2017
Primary completion
Mar 9, 2019
Completion
Apr 4, 2019
Last update posted
Aug 2, 2020

2017 – 2019

United States locations

U.S. sites
22
U.S. states
17
U.S. cities
19
Facility City State ZIP Site status
Banner University Medical Center - Tucson Tucson Arizona 85719
Cedars-Sinai Medical Center Los Angeles California 90048
UCLA Medical Center Los Angeles California 90095
St. Joseph Health Hospital Orange California 92868
Christiana Care Newark Delaware 19713
Baptist Hospital of Miami Miami Florida 33176
AdventHealth Tampa Tampa Florida 33613
Grady Health System Atlanta Georgia 30303
Rush University Medical Center Chicago Illinois 60612
University of Chicago Chicago Illinois 60637
University of Kansas Medical Center Kansas City Kansas 66160
Our Lady of the Lake Hospital Inc. Baton Rouge Louisiana 70808
Detroit Medical Center Detroit Michigan 48201
University of Minnesota Medical Center Minneapolis Minnesota 55455
Mercy Hospital South St Louis Missouri 63128
New York University (NYU) Langone Medical Center New York New York 10016
Mount Sinai New York New York 10029
North Carolina Heart and Vascular Research (NCHVR) Raleigh North Carolina 27607
University of Pennsylvania Medical Center (UPMC) Pittsburgh Pennsylvania 16148
Sanford Health Sioux Falls South Dakota 57117
Sentara Vascular Specialists Norfolk Virginia 23507
Charleston Area Medical Center (CAMC) Charleston West Virginia 25309

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03218566, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 2, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03218566 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →