Prospective Evaluation of Chronic Pancreatitis for Epidemiologic and Translational Studies - PROCEED Study

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

The Coordinating and Data Management Center (CDMC) at MD Anderson Cancer will be responsible for the coordination and data management for the Prospective Evaluation of Chronic Pancreatitis for Epidemiologic and Translational Studies (PROCCEED) Study, which is part of the NIH U01 funded Consortium for the Study of Chronic Pancreatitis, Diabetes, and Pancreatic Cancer (CPDPC). No patient enrollment will occur at MDACC. All patient recruitment will occur at external sites that are a part of the CPDPC. The data management systems, auditing, and monitoring effort are supported by the MD Anderson Cancer Center Clinical Research Support Center (CRSC). PROCEED is the first study in the USA that is carefully following participants to better understand factors that may be responsible for causing pancreatitis and how it progresses. The study is being conducted at the following 9 major clinical centers across the US: * Baylor College of Medicine * Cedars-Sinai Medical Center * University of Florida * Indiana University * Mayo Clinic * University of Minnesota * Ohio State University * Stanford University * University of Pittsburgh The study is enrolling participants who are at different stages of chronic pancreatitis, including those with no known pancreas disease (controls), and those with abdominal pain, one or more attacks of pancreatitis, or chronic pancreatitis. After enrollment, participants with abdominal pain and pancreatitis are asked to follow-up every year to learn about their symptoms and any changes in the disease. PROCEED investigators plan to use the detailed information they collect to better understand the disease and identify new treatments. More details and updated information about this study can be found at the study's public website: https://www.cpdpc-research-consortium.org/research- study-cpdpc-16-02-proceed.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• 1\. Participants with chronic pancreatitis.

Locations
United States
Texas
University of Texas MD Anderson Cancer Center
RECRUITING
Houston
Contact Information
Primary
Li Liang, PHD
lli15@mdanderson.org
713-563-4276
Time Frame
Start Date: 2017-02-28
Estimated Completion Date: 2030-06-30
Participants
Target number of participants: 2345
Treatments
Observational cohort study of adult patients with suspected or definite CP
* Chronic Upper Abdominal Pain of Suspected Pancreatic Origin~* Suspected Chronic Pancreatitis (Patients with Acute Pancreatitis, Recurrent Acute Pancreatitis, or Indeterminate CP without prior AP)~* Definite Chronic Pancreatitis~* Chronic Abdominal Pain- Undifferentiated Group
Authors
Ziding Feng
Sponsors
Leads: M.D. Anderson Cancer Center
Collaborators: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Indiana University, Mayo Clinic, University of Florida, Stanford University, Cedars-Sinai Medical Center, National Institutes of Health (NIH), University of Pittsburgh Medical Center, Ohio State University, Baylor College of Medicine, Kaiser Permanente, University of Minnesota

This content was sourced from clinicaltrials.gov