Patient Guide: G7 Freedom Constrained Vivacit-E Liners

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 10 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05587244
Status: ENROLLING_BY_INVITATION
Condition: Osteoarthritis, Hip, Rheumatoid Arthritis, Non-Union Fracture, Trochanteric Fractures, Femoral Neck Fractures, Avascular Necrosis, Dislocation, Hip
Phase: NA

Where You Can Participate

This study is available at 10 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Los Angeles, California
  • • Gainesville, Florida
  • • And 7 more locations

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G7 Freedom Constrained Vivacit-E Liners - Join Clinical Trial NCTNCT05587244

How to Join This Clinical Trial - NCTNCT05587244

Learn how to participate in this NA trial studying an investigational therapy for Osteoarthritis, Hip, Rheumatoid Arthritis, Non-Union Fracture, Trochanteric Fractures, Femoral Neck Fractures, Avascular Necrosis, Dislocation, Hip. Current status: ENROLLING_BY_INVITATION.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Osteoarthritis, Hip, Rheumatoid Arthritis, Non-Union Fracture, Trochanteric Fractures, Femoral Neck Fractures, Avascular Necrosis, Dislocation, Hip. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Osteoarthritis, Hip, Rheumatoid Arthritis, Non-Union Fracture, Trochanteric Fractures, Femoral Neck Fractures, Avascular Necrosis, Dislocation, Hip
Treatment Being Tested
Investigational treatment
Study Phase
NA - Research study
Enrollment Status
ENROLLING_BY_INVITATION
Study Identifier
NCTNCT05587244 - 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 10 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35205 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90033 - United States

Status: Contact for availability

Clinical Research Site

Gainesville, Florida 32611 - United States

Status: Contact for availability

Clinical Research Site

Livingston, New Jersey 07039 - United States

Status: Contact for availability

Clinical Research Site

Columbus, Ohio 43201 - United States

Status: Contact for availability

Clinical Research Site

Knoxville, Tennessee 37923 - United States

Status: Contact for availability

Clinical Research Site

Houston, Texas 77030 - United States

Status: Contact for availability

Clinical Research Site

Plano, Texas 75075 - United States

Status: Contact for availability

Clinical Research Site

Salt Lake City, Utah 84108 - United States

Status: Contact for availability

Clinical Research Site

Morgantown, West Virginia 26506 - United States

Status: Contact for availability

How to Enroll in This Study

To learn more about participating in this NA clinical trial for Osteoarthritis, Hip, Rheumatoid Arthritis, Non-Union Fracture, Trochanteric Fractures, Femoral Neck Fractures, Avascular Necrosis, Dislocation, Hip:

  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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