Clinical Investigation of the GORE® Drug-Coated PTA Balloon Catheter (GORE® DCB Catheter)

PAD Clinical Trial

— DCB  

Official title:

Clinical Investigation of the GORE® Drug-Coated PTA Balloon Catheter (GORE® DCB Catheter) for Conformité Européene (CE) Mark Approval

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02907203
• Other study ID #: DCB 15-02
• Status: Completed
• Start date: October 10, 2017
• Est. completion date: March 22, 2022

Study information

• Verified date: January 2023
• Source: W.L.Gore & Associates
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will assess the safety and performance of the Gore drug-coated balloon in the treatment of de novo and restenotic atherosclerotic lesions in the superficial femoral and popliteal arteries of patients with symptomatic PAD.

Description:

The primary objective of the clinical investigation is to evaluate the safety and performance of the Gore drug-coated balloon in the treatment of de novo and restenotic atherosclerotic lesions in the superficial femoral and popliteal arteries (SFA/PA) of patients with symptomatic PAD.

The performance of the GORE® DCB Catheter is superior to a performance goal derived from literature reports of uncoated PTA balloons, measured six months after intervention.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 52
• Est. completion date: March 22, 2022
• Est. primary completion date: March 22, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years and older

Eligibility

Inclusion Criteria:

• PAD patients with Rutherford Class 2 - 4

• De novo or restenotic lesions, including total occlusions of the SFA/PA

• 1 lesion which may include one or more regions of luminal narrowing =70% with a total combined lesion length between 30 - 150mm and a reference vessel diameter of 4 - 6mm

• 1 patent tibial or peroneal artery

Exclusion Criteria:

• Surgical or endovascular access in the Target limb/vessel within the previous 30 days

• Prior treatment of the Target lesion with PTA within 90 days or any prior treatment with drug-coated balloon

• Prior treatment of the Target vessel with stenting or bypass

• Iliac artery inflow lesions that cannot be successfully treated during the Index procedure

• Acute or subacute thrombus or arterial aneurysm in Target limb

• Severe calcification that renders the Target lesion non-dilatable

• Acute or chronic renal dysfunction (serum creatinine =2.5 mg/dL)

Related Conditions & MeSH terms

• PAD

Intervention

Device:
• Drug Coated Balloon
Prospective, multi-center, single-arm study characterizing outcomes in subjects with Peripheral Artery Disease (PAD) lesions treated with percutaneous transluminal angioplasty (PTA) using the GORE® DCB Catheter.

Locations

Country	Name	City	State
Germany	Universitats - Herzzentrum Freiburg	Bad Krozingen

Sponsors (1)

Lead Sponsor	Collaborator
W.L.Gore & Associates

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Late Lumen Loss (LLL)	Six month late lumen loss (LLL) is defined as the difference in minimum lumen diameter of the Target lesion between the time points immediately post-intervention and the 6-month follow-up angiography or at the time of a Clinically Driven Target Lesion Revascularization (CD TLR), whichever is earlier.	Six months
Secondary	Number of Subjects With Freedom From Major Adverse Events	A composite 30-day safety endpoint of freedom from Major Adverse Events (MAE), defined as i) death, ii) Clinically-Driven Target Vessel Revascularization (CD TVR), or iii) amputation above the metatarsals, resulting from a vascular event, in the treated leg (Target limb amputation).	30 days