CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 123 enrolled
Drug / intervention
Boston Scientific Ranger™ and Ranger™ SL Paclitaxel-Coated PTA Balloon Catheterdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02944071
NCT02944071N/ACompleted

Prospective, Non-randomized, Multicenter Clinical Study of the Boston Scientific Paclitaxel-Coated PTA Balloon Catheter (Ranger™ and Ranger™ SL (OTW) DCB) in China

Boston Scientific Corporation·interventional·Posted Oct 25, 2016·Updated Oct 27, 2025

In Brief

A clinical study evaluating Boston Scientific Ranger™ and Ranger™ SL Paclitaxel-Coated PTA Balloon Catheter for Femoropopliteal Artery Lesions. Completed, enrolled 123 participants across 9 sites.

Detailed Summary

This clinical study is a prospective, non-randomized, multicenter study to demonstrate the acceptable safety and performance of angioplasty with the Ranger DCB in native femoropopliteal artery lesions. It is intended that all patients with qualifying lesions would be considered for enrollment and treated with the Ranger DCB catheter. Approximately 123 patients with femoropopliteal artery lesions will be enrolled. All lesions will be treated with the Ranger DCB. Up to 15 clinical sites located in China are expected to participate.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedOct 25, 2016
Enrollment StartNov 24, 2016
Primary CompletionDec 22, 2020
TodayJul 2, 2026
Enrollment to primary: 4.1 yearsPosted 9.7 years ago

Interventions

Boston Scientific Ranger™ and Ranger™ SL Paclitaxel-Coated PTA Balloon Catheterdevice