Viewing Study NCT05780359



Ignite Creation Date: 2024-05-06 @ 6:47 PM
Last Modification Date: 2024-10-26 @ 2:54 PM
Study NCT ID: NCT05780359
Status: RECRUITING
Last Update Posted: 2023-03-22
First Post: 2023-03-08

Brief Title: Evaluating the Safety and Efficacy of the G-stream Drug-Eluting Stent in the Above-the-Knee Femoropopliteal Artery
Sponsor: Shenzhen Salubris Pharmaceuticals Co Ltd
Organization: Shenzhen Salubris Pharmaceuticals Co Ltd

Study Overview

Official Title: A Multicenter Randomized Controlled Superiority Clinical Trial to Evaluate the Safety and Efficacy of Drug-eluting Peripheral Arterial Stent SystemG-stream in the Treatment of the Above-the-knee Femoropopliteal Artery Stenosis or Occlusion
Status: RECRUITING
Status Verified Date: 2023-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: G-streamPAD
Brief Summary: A multicenter randomized controlled superiority clinical trial to evaluate the efficacy and safety of drug-eluting peripheral arterial stent systemG-stream in the treatment of femoropopliteal artery stenosis or occlusion
Detailed Description: To evaluate the efficacy and safety of the drug-eluting peripheral arterial stent systemG-stream in the treatment of superficial femoral artery andor proximal popliteal artery Taking the drug eluting balloon catheter AcoArt-Orchid as control

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None