Patient Guide: A Longitudinal Observational Study of Patients With Nonalcoholic Steatohepatitis (NASH) and Related Conditions Across the Entire Spectrum of Nonalcoholic Fatty Liver Disease (NAFLD)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 74 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT02815891
Status: 🟢 Enrolling Now
Condition: Nonalcoholic Fatty Liver, Nonalcoholic Steatohepatitis
Phase: Not Specified

Where You Can Participate

This study is available at 74 locations across the country.

Top locations include:
  • • Phoenix, Arizona
  • • Palo Alto, California
  • • Pasadena, California
  • • And 71 more locations

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A Longitudinal Observational Study of Patients With Nonalcoholic Steatohepatitis (NASH) and Related Conditions Across the Entire Spectrum of Nonalcoholic Fatty Liver Disease (NAFLD) - Join Clinical Trial NCTNCT02815891

How to Join This Clinical Trial - NCTNCT02815891

Learn how to participate in this Not Specified trial studying an investigational therapy for Nonalcoholic Fatty Liver, Nonalcoholic Steatohepatitis. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Nonalcoholic Fatty Liver, Nonalcoholic Steatohepatitis
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT02815891 - 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 74 locations. Find a study site near you:

Clinical Research Site

Phoenix, Arizona 85006 - United States

Status: TERMINATED

Clinical Research Site

Palo Alto, California 94304 - United States

Status: TERMINATED

Clinical Research Site

Pasadena, California 91105 - United States

Status: TERMINATED

Clinical Research Site

Sacramento, California 95817 - United States

Status: TERMINATED

Clinical Research Site

San Jose, California 95128 - United States

Status: TERMINATED

Clinical Research Site

Aurora, Colorado 80045 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Hartford, Connecticut 06105 - United States

Status: TERMINATED

Clinical Research Site

Hartford, Connecticut 06106 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Washington, District of Columbia 20007 - United States

Status: TERMINATED

Clinical Research Site

Clearwater, Florida 33762 - United States

Status: ACTIVE_NOT_RECRUITING

And 64 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Nonalcoholic Fatty Liver, Nonalcoholic Steatohepatitis:

  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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