Clinical trial
A Prospective, Multicenter and Randomized Controlled Trial to Evaluate the Efficacy and Safety of Sperstent® Peripheral Spot Stent System Used for the Residual Lesions After Percutaneous Transluminal Angioplasty of Femoropopliteal Arteries
NCT06539689 is registered in ClinicalTrials.gov with FrontAce Scientific Co., Ltd as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Prospective, Multicenter and Randomized Controlled Trial to Evaluate the Efficacy and Safety of Sperstent® Peripheral Spot Stent System Used for the Residual Lesions After Percutaneous Transluminal Angioplasty of Femoropopliteal Arteries
- Lead sponsor
- FrontAce Scientific Co., Ltd
- Phase
- Not applicable
- Overall status
- Recruiting
- Start date
- June 4, 2024
- Completion date
- December 31, 2026
- Enrollment
- 240 (estimated)
- Sites
- 12
Conditions
As the registry lists them; a condition with its own page is linked.
dissection, peripheral arterial disease, stenosis