Patient Guide: Evaluation of the Safety and Effectiveness of ARTIA Reconstructive Tissue Matrix Breast Reconstruction (ADORA) in Adult Participants

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 12 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06575192
Status: 🟢 Enrolling Now
Condition: Breast Reconstruction
Phase: PHASE3

Where You Can Participate

This study is available at 12 locations across the country.

Top locations include:
  • • Orange, California
  • • Torrance, California
  • • Northbrook, Illinois
  • • And 9 more locations

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Evaluation of the Safety and Effectiveness of ARTIA Reconstructive Tissue Matrix Breast Reconstruction (ADORA) in Adult Participants - Join Clinical Trial NCTNCT06575192

How to Join This Clinical Trial - NCTNCT06575192

Learn how to participate in this PHASE3 trial studying an investigational therapy for Breast Reconstruction. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Breast Reconstruction
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06575192 - 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 12 locations. Find a study site near you:

Clinical Research Site

Orange, California 92868-3201 - United States

Status: RECRUITING

Clinical Research Site

Torrance, California 90505-3927 - United States

Status: RECRUITING

Clinical Research Site

Northbrook, Illinois 60062-2802 - United States

Status: RECRUITING

Clinical Research Site

Saint Louis, Missouri 63130 - United States

Status: RECRUITING

Clinical Research Site

Las Vegas, Nevada 89154 - United States

Status: RECRUITING

Clinical Research Site

Newark, New Jersey 07103 - United States

Status: RECRUITING

Clinical Research Site

New York, New York 10016-6402 - United States

Status: COMPLETED

Clinical Research Site

Columbus, Ohio 43202 - United States

Status: RECRUITING

Clinical Research Site

Chattanooga, Tennessee 37403 - United States

Status: RECRUITING

Clinical Research Site

Houston, Texas 77030 - United States

Status: RECRUITING

And 2 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Breast Reconstruction:

  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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