GBPDC: Gut-Brain in PD Consortium Master Protocol

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age21-80
SponsorDuke University

About this trial

The purpose of this research study is to identify the role that the gut-brain axis, the group of nerves that connect the brain and gut, plays in Parkinson's disease (PD). The National Institute of Diabetes and Digestive and Kidney Diseases is sponsoring this research study.

During this study, specific groups of participants, also known as "cohorts", will be identified based on the severity of their PD. There will also be a cohort enrolling participants who do not have Parkinson's and a cohort enrolling participants that are at risk for developing PD. Each of these cohorts will be compared to the others to assess the differences in the gut-brain connection.

Participants in this study will:

* meet with a medical provider * answer questionnaires * give samples of blood, stool, and saliva * have X-rays taken while swallowing different foods (swallowing study) * have X-rays taken to see how long it takes markers to move through their colon (colon transit study) * have a flexible sigmoidoscopy, where a doctor looks inside the lower part of the colon and takes small tissue samples (biopsies) from the mucosa (lining) * have samples taken of their skin * have an anorectal manometry and a balloon expulsion test, where a small tube and balloon are placed in the rectum to measure muscle function.

Participation in the study will last up to 24 months (2 years).

Eligibility criteria

Qualifiers

Aged ≥21 years old and ≤80 years old

Clinical diagnosis of PD as defined by Movement Disorder Society (MDS) PD Criteria

Adequate visual, hearing, cognitive, and physical ability

Willingness and ability to comply with scheduled visits, laboratory tests, and other study procedures. Because longitudinal participation is important to the scientific goals of the program, a "best estimate" of interest, commitment, and geographic feasibility for three years will be documented by the enrolling investigator after interview with the potential enrollee

Disqualifiers

Diagnosis of secondary or atypical parkinsonism

Hemoglobin (Hgb) <10

Platelets <70,000

Alanine Transaminase (ALT) or Aspartate Aminotransferase (AST) > 2 1/2 times upper limit of normal (ULN)

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

250 Participants
are grouped into 3 trial groups

Sponsors and collaborators

Duke University

Lead sponsor

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborator

University of Chicago

Collaborator

Rush University Medical Center

Collaborator

Massachusetts General Hospital

Collaborator

Stanford University

Collaborator

Medical University of South Carolina

Collaborator

Columbia University

Collaborator

Mayo Clinic

Collaborator