This study is currently not recruiting participants.

Clinical Evaluation of the Absorb? Bioresorbable Vascular Scaffold (BVS) System in the Treatment of Subjects with de novo Native Coronary Artery Lesions

Study on the Treatment of Coronary Artery Blockages with an Investigational Device

Not Recruiting
18 years - 100 years
All
Phase N/A

Brief description of study.

The purpose of this Study is to assess the safety and effectiveness of treating blockages in the coronary (heart) arteries (blood vessels) with an investigational device called Absorb? Bioresorbable Vascular Scaffold (BVS) System (the ?Absorb BVS?), compa

Detailed description of study

The purpose of this Study is to assess the safety and effectiveness of treating blockages in the coronary (heart) arteries (blood vessels) with an investigational device called Absorb? Bioresorbable Vascular Scaffold (BVS) System (the ?Absorb BVS?), compa

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Native Coronary Artery Lesions
  • Age: 18 years - 100 years
  • Gender: All

This study investigates the treatment of blockages in the coronary arteries using an investigational device. Coronary arteries are the blood vessels that supply blood to the heart. The investigational device is being compared to standard treatments to determine its safety and effectiveness.

Participants will undergo procedures that involve the use of the investigational device to treat their coronary artery blockages. The study will monitor the participants closely to assess how well the device works and to check for any side effects.

  • Who can participate: Adults aged 18 and older with diagnosed coronary artery blockages may be eligible to participate. Key eligibility factors include having a blockage that can be treated with the investigational device and meeting specific health criteria.
  • Study details: Participants will receive treatment for their coronary artery blockages using an investigational device. The study will involve regular monitoring to assess the device's effectiveness and safety.
Updated on 19 Feb 2024. Study ID: 1305011374

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