Patient Guide: Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh

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: NCTNCT04779918
Status: 🟢 Enrolling Now
Condition: Hernia, Ventral, Hernia, Inguinal
Phase: NA

Where You Can Participate

This study is available at 10 locations across the country.

Top locations include:
  • • Mobile, Alabama
  • • Denver, Colorado
  • • Destin, Florida
  • • And 7 more locations

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Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh - Join Clinical Trial NCTNCT04779918

How to Join This Clinical Trial - NCTNCT04779918

Learn how to participate in this NA trial studying an investigational therapy for Hernia, Ventral, Hernia, Inguinal. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Hernia, Ventral, Hernia, Inguinal
Treatment Being Tested
Investigational treatment
Study Phase
NA - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT04779918 - 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

Mobile, Alabama 36617 - United States

Status: RECRUITING

Clinical Research Site

Denver, Colorado 802210 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Destin, Florida 325541 - United States

Status: TERMINATED

Clinical Research Site

Fort Myers, Florida 33912 - United States

Status: TERMINATED

Clinical Research Site

Overland Park, Kansas 66213 - United States

Status: RECRUITING

Clinical Research Site

Louisville, Kentucky 40202 - United States

Status: RECRUITING

Clinical Research Site

Traverse City, Michigan 49684 - United States

Status: RECRUITING

Clinical Research Site

Roslyn, New York 11576 - United States

Status: WITHDRAWN

Clinical Research Site

Utica, New York 13502 - United States

Status: RECRUITING

Clinical Research Site

Houston, Texas 77030 - United States

Status: ACTIVE_NOT_RECRUITING

How to Enroll in This Study

To learn more about participating in this NA clinical trial for Hernia, Ventral, Hernia, Inguinal:

  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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