Patient Guide: Single-Patient Expanded Access Protocol for Tradipitant In A Single Patient With Gastroparesis

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 15 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04474990
Status: AVAILABLE
Condition: Gastroparesis, Diabetic Gastroparesis
Phase: Not Specified

Where You Can Participate

This study is available at 15 locations across the country.

Top locations include:
  • • Maitland, Florida
  • • Tampa, Florida
  • • Wauconda, Illinois
  • • And 12 more locations

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Single-Patient Expanded Access Protocol for Tradipitant In A Single Patient With Gastroparesis - Join Clinical Trial NCTNCT04474990

How to Join This Clinical Trial - NCTNCT04474990

Learn how to participate in this Not Specified trial studying an investigational therapy for Gastroparesis, Diabetic Gastroparesis. Current status: AVAILABLE.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Gastroparesis, Diabetic Gastroparesis
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
AVAILABLE
Study Identifier
NCTNCT04474990 - 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 15 locations. Find a study site near you:

Clinical Research Site

Maitland, Florida 32751 - United States

Status: AVAILABLE

Clinical Research Site

Tampa, Florida 33613 - United States

Status: AVAILABLE

Clinical Research Site

Wauconda, Illinois 60084 - United States

Status: AVAILABLE

Clinical Research Site

Wichita, Kansas 67214 - United States

Status: AVAILABLE

Clinical Research Site

Louisville, Kentucky 40202 - United States

Status: AVAILABLE

Clinical Research Site

Chevy Chase, Maryland 20815 - United States

Status: AVAILABLE

Clinical Research Site

Boston, Massachusetts 02215 - United States

Status: AVAILABLE

Clinical Research Site

Chesterfield, Missouri 63005 - United States

Status: AVAILABLE

Clinical Research Site

Charlotte, North Carolina 28209 - United States

Status: AVAILABLE

Clinical Research Site

Tulsa, Oklahoma 74104 - United States

Status: AVAILABLE

And 5 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 Gastroparesis, Diabetic Gastroparesis:

  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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