🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT04511247
Recruiting Not applicable

SirolimUs CoaTed Balloon for The TrEatment of Below The Knee Arterial Disease

NCT04511247 · tracked via the Priya Life Science China tracker
Sponsor
Concept Medical Inc.
Phase
Not applicable
Started
2020-08-15
Last updated
2025-07-03

Condition(s) studied

Peripheral Artery DiseaseAtherosclerosisArterial Disease of Legs

Investigational drug(s) / intervention(s)

MagicTouch PTA Sirolimus drug coated balloonPOBA balloon

MagicTouch PTA Sirolimus drug coated balloon: For participants randomised to MagicTouch PTA sirolimus DCB, following successful plain balloon angioplasty of the arterial lesion (defined as \<30% residual stenosis after treatment at rated burst pressure of the angioplasty balloon), MagicTouch sirolimus coated balloon will be applied at the lesion after appropriate sizing using the diameter of the plain balloon angioplasty.

POBA balloon: For participants randomised to the standard balloon angioplasty group, a placebo standard balloon which is identical to the SCB will also be applied at the lesion after appropriate sizing using the diameter of the plain balloon angioplasty

Study summary

This study aims to conduct a randomized, double blind, randomised controlled multicentre trial of sirolimus drug coated balloon versus standard percutaneous transluminal angioplasty for the treatment of below the knee arterial disease.

Eligibility

Sex
ALL
Min age
21 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥ 21 years or minimum age 2. Rutherford class 4 to 6 in the target limb Intraoperative Inclusion Criteria 3. Single or sequential de novo or re-stenotic lesions (stenosis of \> 50% or occlusions) from 2 to 20cm in the proximal 200mm of below the knee arteries. Lesion is considered as one lesion if there is maximum of 30mm gap between lesions at discretion of investigator. Below the knee arteries are tibioperoneal trunk, anterior tibial artery, posterior tibial artery and peroneal artery 4. Inflow free from flow limiting lesions (\<50% stenosis) confirmed by duplex or angiography. Subjects with flow limiting inflow lesions (\>50% stenosis) can be included if lesion had been treated successfully (\<30% residual stenosis) before or during the index procedure. 5. Target vessel has angiographically documented run off to the foot after treatment (ie. without significant stenosis) Exclusion Criteria: 1. Comorbid conditions limiting life expectancy ≤ 1 year 2. Subject is currently participating in another investigational drug or device study that has not reached first primary endpoint yet 3. Subject is pregnant or planning to become pregnant during the course of the study 4. Heel gangrene 5. Prior bypass surgery of target vessel 6. Planned amputation of the target limb 7. Previously implanted stent in the target lesion 8. Vulnerable or protected adults 9. Bleeding diathesis or another disorder such as gastrointestinal ulceration which restrict the use of clopidogrel or aspirin 10. Known allergy to sirolimus Intraoperative Exclusion Criteria 11. Failure to successfully cross the target lesion with a guide wire (successful crossing means tip of the guide wire distal to the target lesion in the absence of flow limiting dissections or perforations). 12. Target vessel has lesions extending beyond the ankle joint 13. Failure to obtain \<30% residual stenosis in a pre-existing lesion 14. Lesions requiring retrograde access (SAFARI) 15. Highly calcified lesions (Contiguous calcification on both sides of the lesion) 16. Use of DCBs, drug eluting stent, specialty balloons or artherectomy devices during the index procedure. (Non-compliant balloons are not considered specialty balloons)

Primary outcome measure(s)

Trial sites (20)

FacilityCityRegionStatus
Khoo Teck Puat Hospital Singapore Singapore Recruiting
National University Hospital Singapore Singapore Recruiting
Ng Teng Fong General Hospital Singapore Singapore Not Yet Recruiting
Sengkang General Hospital Singapore Singapore Recruiting
Singapore General Hospital Singapore Singapore Recruiting
Tan Tock Seng Hospital Singapore Singapore Recruiting
Kaohsiung Medical University Chung-Ho Memorial Hospital Kaohsiung City Taiwan Recruiting
Kaoshiung Chang Gung Memorial Hospital Kaohsiung City Taiwan Recruiting
Far Eastern Memorial Hospital New Taipei City Taiwan Recruiting
Taipei Tzuchi Hospital New Taipei City Taiwan Recruiting
China Medical University Hospital Taichung Taiwan Not Yet Recruiting
National Taiwan University Hospital Taipei Taiwan Recruiting
Shin Kong Wu Ho-Su Memorial Hospital Taipei Taiwan Recruiting
Linkou Chang Gung Memorial Hospital Taoyuan City Taiwan Recruiting
Phramongkutklao Hospital Bangkok Thailand Recruiting
Rajavithi Hospital Bangkok Thailand Recruiting
Ramathibodi Hospital Bangkok Thailand Not Yet Recruiting
Siriraj Hospital Bangkok Thailand Recruiting
Vajira Hospital Bangkok Thailand Recruiting
Thammasat University Hospital Pathum Thani Thailand Recruiting

More Concept Medical Inc. trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04511247 on ClinicalTrials.gov ↗ ← All trials in China