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Enrolling by invitation No phase listed Observational

The Percutaneous Transmural Arterial Bypass -1 Study (Post Approval Registry)

ClinicalTrials.gov ID: NCT06315023

Public ClinicalTrials.gov record NCT06315023. 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 28, 2026, 4:10 AM EDT

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

Official title

Prospective, Single Arm, Registry-based Study to Evaluate the Real-world Use of the DETOUR™ System in US Patients

Brief summary

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

The purpose of this post-market surveillance study will be to evaluate the real-world use of the DETOUR System in treated patients with symptomatic femoropopliteal lesions from 200 mm to 460 mm in length with chronic total occlusions (100 mm to 425 mm) or diffuse stenosis \> 70% who may be considered suboptimal candidates for surgical or alternative endovascular treatments.

Study identification

NCT ID
NCT06315023
Recruitment status
Enrolling by invitation
Study type
Observational
Phase
Not listed
Lead sponsor
Endologix
Industry
Enrollment
450 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
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
Oct 5, 2023
Primary completion
Jun 6, 2028
Completion
Jun 6, 2032
Last update posted
May 11, 2026

2023 – 2032

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
Salinas Valley Memorial Hospital Salinas California 93901 —
University of Connecticut Storrs Connecticut 06269 —
Medstar Washington Hospital Center Washington D.C. District of Columbia 20010 —
Delray Medical Center Delray Beach Florida 33484 —
Beth Isreal Deaconess Medical Center Boston Massachusetts 02215 —
Saint Luke's Hospital of Kansas City Kansas City Missouri 64111 —
NYU Langone Medical Center New York New York 10016 —
Cleveland Clinic Main Campus Cleveland Ohio 44195 —
University of Pennsylvania West Chester Pennsylvania 19380 —
Main Line Health Wynnewood Pennsylvania 19096 —

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 NCT06315023, 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 May 11, 2026 · Synced Sep 28, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06315023 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →