Patient Guide: Post-approval Registry Study to Evaluate the Continued Safety and Probable Benefit of the MID-C System for 5 Years Post-Implantation in Adolescent Idiopathic Scoliosis (AIS)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 14 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04296903
Status: ACTIVE_NOT_RECRUITING
Condition: Adolescent Idiopathic Scoliosis
Phase: NA

Where You Can Participate

This study is available at 14 locations across the country.

Top locations include:
  • • San Diego, California
  • • Jacksonville, Florida
  • • Atlanta, Georgia
  • • And 11 more locations

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Post-approval Registry Study to Evaluate the Continued Safety and Probable Benefit of the MID-C System for 5 Years Post-Implantation in Adolescent Idiopathic Scoliosis (AIS) - Join Clinical Trial NCTNCT04296903

How to Join This Clinical Trial - NCTNCT04296903

Learn how to participate in this NA trial studying an investigational therapy for Adolescent Idiopathic Scoliosis. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Adolescent Idiopathic Scoliosis
Treatment Being Tested
Investigational treatment
Study Phase
NA - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04296903 - 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 14 locations. Find a study site near you:

Clinical Research Site

San Diego, California 92123 - United States

Status: Contact for availability

Clinical Research Site

Jacksonville, Florida 32207 - United States

Status: Contact for availability

Clinical Research Site

Atlanta, Georgia 30060 - United States

Status: Contact for availability

Clinical Research Site

Indianapolis, Indiana 46202 - United States

Status: Contact for availability

Clinical Research Site

Kansas City, Kansas 64108 - United States

Status: Contact for availability

Clinical Research Site

Rochester, Minnesota 55902 - United States

Status: Contact for availability

Clinical Research Site

Jackson, Mississippi 39216 - United States

Status: Contact for availability

Clinical Research Site

Columbia, Missouri 65201 - United States

Status: Contact for availability

Clinical Research Site

St Louis, Missouri 63110 - United States

Status: Contact for availability

Clinical Research Site

New York, New York 10029 - United States

Status: Contact for availability

And 4 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this NA clinical trial for Adolescent Idiopathic Scoliosis:

  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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