Patient Guide: A Non-interventional Implementation Study to Evaluate Treatment With Inclisiran (Leqvio®) and Other Lipid Lowering Treatments in a Real-world Setting

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 122 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05362903
Status: ACTIVE_NOT_RECRUITING
Condition: Hypercholesterolemia
Phase: Not Specified

Where You Can Participate

This study is available at 122 locations across the country.

Top locations include:
  • • Freudenstadt, Baden Wuerttemberg
  • • Heidelberg, Baden Wuerttemberg
  • • Kirchheim Unter Teck, Baden-Wuerttemberg
  • • And 119 more locations

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A Non-interventional Implementation Study to Evaluate Treatment With Inclisiran (Leqvio®) and Other Lipid Lowering Treatments in a Real-world Setting - Join Clinical Trial NCTNCT05362903

How to Join This Clinical Trial - NCTNCT05362903

Learn how to participate in this Not Specified trial studying an investigational therapy for Hypercholesterolemia. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Hypercholesterolemia
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05362903 - 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 122 locations. Find a study site near you:

Clinical Research Site

Freudenstadt, Baden Wuerttemberg 72250 - Germany

Status: Contact for availability

Clinical Research Site

Heidelberg, Baden Wuerttemberg 69115 - Germany

Status: Contact for availability

Clinical Research Site

Kirchheim Unter Teck, Baden-Wuerttemberg 73230 - Germany

Status: Contact for availability

Clinical Research Site

Konstanz, Baden-Wuerttemberg 78464 - Germany

Status: Contact for availability

Clinical Research Site

Coburg, Bavaria 96450 - Germany

Status: Contact for availability

Clinical Research Site

Deggendorf, Bavaria 94469 - Germany

Status: Contact for availability

Clinical Research Site

Muenchen, Bavaria 80939 - Germany

Status: Contact for availability

Clinical Research Site

Wuerzburg, Bavaria 97080 - Germany

Status: Contact for availability

Clinical Research Site

Dachau, Bayern 85221 - Germany

Status: Contact for availability

Clinical Research Site

Fuessen, Bayern 87629 - Germany

Status: Contact for availability

And 112 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Hypercholesterolemia:

  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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