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Completed Not applicable Interventional Results available

FORWARD PAD IDE Study With the Shockwave Javelin IVL Catheter

ClinicalTrials.gov ID: NCT05858905

Public ClinicalTrials.gov record NCT05858905. 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 Sep 2, 2026, 3:59 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

Forward-Shifted Intravascular Lithotripsy (IVL) Technology in a Prospective, Multi-center, Single-arm Investigational Device Exemption (IDE) Study

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The FORWARD PAD IDE Study is a prospective, multi-center, single-arm investigational device exemption study, conducted to assess the safety and effectiveness of the Shockwave Medical Mini S Peripheral IVL System for the treatment of heavily calcified, stenotic peripheral arteries.

Study identification

NCT ID
NCT05858905
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Shockwave Medical, Inc.
Industry
Enrollment
75 participants

Conditions and interventions

Interventions

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
Jun 26, 2023
Primary completion
Apr 4, 2024
Completion
Apr 20, 2025
Last update posted
Jul 13, 2026

2023 – 2025

United States locations

U.S. sites
21
U.S. states
17
U.S. cities
21
Facility City State ZIP Site status
Stanford Hospital and Clinics (SHC) Palo Alto California 94304
Advanced Heart and Vein Center Thornton Colorado 80023
HCA Florida Blake Hospital Bradenton Florida 34209
Tallahassee Memorial Healthcare, Inc. Tallahassee Florida 32308
UnityPoint Health Trinity Bettendorf Hospital Bettendorf Iowa 52722
Cardiovascular Medicine PC Davenport Iowa 52803
MedStar Montgomery Medical Center Olney Maryland 20832
Southcoast Hospitals Group New Bedford Massachusetts 02740
North Mississippi Medical Center Tupelo Mississippi 38801
NYU Langone Health New York New York 10016
Charlotte Radiology Charlotte North Carolina 28202
The Lindner Research Center at The Christ Hospital Cincinnati Ohio 45219
Ascension St. John Jane Phillips Hosptial Bartlesville Oklahoma 74006
Lankenau Institute for Medical Research Bryn Mawr Pennsylvania 19096
The Miriam Hospital Providence Rhode Island 02906
Vanderbilt University Medical Center Nashville Tennessee 37212
University of Texas Southwestern Medical Center Dallas Texas 75390
The Heart Hospital Baylor Plano Texas 75093
Sentara Vascular Specialists Norfolk Virginia 23507
Marshfield Medical Center Marshfield Wisconsin 54449
Ascension Columbia St. Mary's Milwaukee Wisconsin 53211

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 NCT05858905, 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 Jul 13, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05858905 live on ClinicalTrials.gov.

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