Vancomycin and Fecal Microbiota Transplant for Parkinson's Disease
Fecal Microbiota Transplant
Synucleinopathies+6
+ Basal Ganglia Diseases
+ Brain Diseases
Supportive Care Study
Summary
Study start date: July 1, 2026
Actual date on which the first participant was enrolled.This study is looking into the safety of using a treatment combination for adults with Parkinson's disease. It starts with a 10-day course of the antibiotic Vancomycin, followed by a procedure called a fecal microbiota transplant (FMT). The idea is to see if this combination can safely help people with Parkinson's disease, a condition that affects movement and motor skills. This study is important because it explores a potentially new way to care for Parkinson's disease by possibly improving gut health, which might have an effect on the disease's symptoms. Participants in the study will have several scheduled visits and procedures. They will first meet with the study doctor to discuss the study and have initial assessments. After taking Vancomycin, participants will prepare for the FMT procedure, which will be done through a colonoscopy at an outpatient center. Following the FMT, there are multiple follow-up visits to observe and assess participants' well-being. Daily phone check-ins will occur the week after FMT, and weekly calls are made for further monitoring. This approach ensures a comprehensive evaluation of any changes in health, medication, and side effects, aiming to ensure participant safety throughout the study.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.10 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 85 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location