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Genomic Resources for Enhancing Available Therapies (GREAT1.0) Study — GREAT1  

Rheumatoid Arthritis Clinical Trial

Official title:
Genomic Resources for Enhancing Available Therapies (GREAT1.0) Study

Clinical Trial Summary

This is a prospective, descriptive, observational research study designed to observe and document the clinical practice by domain experts, and how the knowledge of new findings that are published in the medical literature affect clinical decision making. The study will evaluate risk factors and co-variants, including genetic variants that are associated with disease progression such as pain, inflammation, organ dysfunction, disability and quality of life.

Clinical Trial Description

The Genomic Resource to Enhance Available Therapies (GREAT1.0) Study is a research program for personalized medicine. It is a highly annotated genetic and biosample resource for multiple nested observational cohort studies. It is designed to begin to understand the mechanisms underlying complex diseases using clinical information from the UPMC electronic health record (EHR), from case-report forms, and from biological samples. Aim 1. To test the hypothesis that point-of-care electronic health record (EHR)-based phenotyping and clinical measures will be useful for classifying patient by disease risk, subtype, activity, complications, quality of life or using statistical or systems approaches. Aim 2. To test the hypothesis that common diseases can be subtyped using genotype data. Aim 3. To test the hypothesis biological samples will provide additional functional and mechanistic information about subject health, disease or state. The study will be conducted using UPMC patients and population controls. Consent will allow EHR and/or case report form data, plus biological samples to be given a unique code number and transferred to researchers for analysis. Consent will also allow for a secure link to be maintained allowing the research data or samples to be updated, and to contact the clinical team and/or subject to provide them with additional information. ;

Study Design

Related Conditions & MeSH terms

  • Acute Pancreatitis
  • Bile Acid Synthesis Defect
  • Biliary Cirrhosis
  • Celiac Disease
  • Cholecystitis
  • Cholelithiases
  • Cholelithiasis
  • Chronic Disease
  • Chronic Kidney Diseases
  • Chronic Pain
  • Chronic Pancreatitis
  • Constipation
  • Constipation - Functional
  • Constipation Chronic Idiopathic
  • Crohn Disease
  • Cyst Pancreas
  • Cystic Fibrosis
  • Diabetes Mellitus
  • Diarrhea
  • Diarrhea Chronic
  • Dyslipidemias
  • Exocrine Pancreatic Insufficiency
  • Fatty Liver
  • Fibrosis
  • Gastritis
  • Hepatitis
  • Inflammatory Bowel Diseases
  • IPMN
  • Irritable Bowel Syndrome
  • Kidney Diseases
  • Liver Cirrhosis, Biliary
  • Multiple Sclerosis
  • NASH - Nonalcoholic Steatohepatitis
  • Non-alcoholic Fatty Liver Disease
  • Pancreatic Exocrine Insufficiency
  • Pancreatitis
  • Pancreatitis, Chronic
  • Renal Insufficiency, Chronic
  • Rheumatoid Arthritis
Clinical Trial Details
NCT number NCT04306939
Study type Observational
Source University of Pittsburgh
Contact
Status Suspended
Phase
Start date November 1, 2014
Completion date December 1, 2025
View Details
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