Patient Guide: Memory Gel and Shape Combined Cohort

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 78 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT02919592
Status: ACTIVE_NOT_RECRUITING
Condition: Primary Breast Augmentation, Primary Breast Reconstruction, Revision Breast Augmentation, Revision Breast Reconstruction
Phase: NA

Where You Can Participate

This study is available at 78 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Tuscaloosa, Alabama
  • • Gilbert, Arizona
  • • And 75 more locations

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Memory Gel and Shape Combined Cohort - Join Clinical Trial NCTNCT02919592

How to Join This Clinical Trial - NCTNCT02919592

Learn how to participate in this NA trial studying an investigational therapy for Primary Breast Augmentation, Primary Breast Reconstruction, Revision Breast Augmentation, Revision Breast Reconstruction. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Primary Breast Augmentation, Primary Breast Reconstruction, Revision Breast Augmentation, Revision 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
Primary Breast Augmentation, Primary Breast Reconstruction, Revision Breast Augmentation, Revision Breast Reconstruction
Treatment Being Tested
Investigational treatment
Study Phase
NA - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT02919592 - 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 78 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35242 - United States

Status: Contact for availability

Clinical Research Site

Tuscaloosa, Alabama 35406 - United States

Status: Contact for availability

Clinical Research Site

Gilbert, Arizona 85295 - United States

Status: Contact for availability

Clinical Research Site

Mesa, Arizona 85297 - United States

Status: Contact for availability

Clinical Research Site

Phoenix, Arizona 85014 - United States

Status: Contact for availability

Clinical Research Site

Scottsdale, Arizona 85260 - United States

Status: Contact for availability

Clinical Research Site

Scottsdale, Arizona 85260 - United States

Status: Contact for availability

Clinical Research Site

Scottsdale, Arizona 85260 - United States

Status: Contact for availability

Clinical Research Site

Fayetteville, Arkansas 72703 - United States

Status: Contact for availability

Clinical Research Site

Beverly Hills, California 90210 - United States

Status: Contact for availability

And 68 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 Primary Breast Augmentation, Primary Breast Reconstruction, Revision Breast Augmentation, Revision 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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