Patient Guide: S-FLEX Netherlands Registry: Prospective Evaluation of the Supraflex Family Sirolimus-eluting Coronary Stent System

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 7 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT03443999
Status: 🟢 Enrolling Now
Condition: Coronary Artery Disease
Phase: Research Study

Where You Can Participate

This study is available at 7 locations across the country.

Top locations include:
  • • Leeuwarden, Friesland
  • • Breda, North Brabant
  • • Eindhoven, North Brabant
  • • And 4 more locations

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S-FLEX Netherlands Registry: Prospective Evaluation of the Supraflex Family Sirolimus-eluting Coronary Stent System - Join Clinical Trial NCTNCT03443999

How to Join This Clinical Trial - NCTNCT03443999

Learn how to participate in this clinical trial studying an investigational therapy for Coronary Artery Disease. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Coronary Artery Disease. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Coronary Artery Disease
Treatment Being Tested
Investigational treatment
Study Phase
Clinical trial phase - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT03443999 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 7 locations. Find a study site near you:

Clinical Research Site

Leeuwarden, Friesland 8934 AD - Netherlands

Status: RECRUITING

Clinical Research Site

Breda, North Brabant 4818 CK Breda - Netherlands

Status: RECRUITING

Clinical Research Site

Eindhoven, North Brabant 5623 EJ - Netherlands

Status: RECRUITING

Clinical Research Site

Blaricum, North Holland 1261 AN - Netherlands

Status: RECRUITING

Clinical Research Site

Dordrecht, South Holland Post bus 444 3300 AK - Netherlands

Status: RECRUITING

Clinical Research Site

Rotterdam, South Holland 3079 DZ - Netherlands

Status: RECRUITING

Clinical Research Site

Terneuzen, Zeeuws- Vlaanderen 4535 PA - Netherlands

Status: RECRUITING

How to Enroll in This Study

To learn more about participating in this clinical trial for Coronary Artery Disease:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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