This study is currently not recruiting participants.

A Multicenter Double-Blind Parallel Group Placebo Controlled Study of Creatine in Subjects with Treated Parkinson's Disease (PD) LS-1

Study on Investigational Medication for Parkinson's Disease Progression

Not Recruiting
18 years - 100 years
All
Phase N/A

Brief description of study.

We are conducting this study to determine if creatine, the study drug, slows the worsening of Parkinson's Disease over time.

Detailed description of study

We are conducting this study to determine if creatine, the study drug, slows the worsening of Parkinson's Disease over time.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Parkinson's Disease
  • Age: 18 years - 100 years
  • Gender: All

This study investigates whether an investigational medication can slow the progression of Parkinson's Disease, a condition that affects movement and can cause tremors, stiffness, and balance problems. The purpose of this study is to understand how the investigational medication impacts the progression of these symptoms over time.

Participants will be randomly assigned to different study arms, where they will either receive the investigational medication or a placebo. A placebo is an inactive substance that looks like the investigational medication but does not contain any medicine. Participants will undergo regular assessments to monitor their condition.

  • Who can participate: Participants must be adults aged 18-75 diagnosed with Parkinson's Disease. Additional eligibility criteria include stable medication regimens and no history of severe psychiatric disorders.
  • Study details: Participants will be placed in different study arms to receive either the investigational medication or a placebo. A placebo is an inactive substance that looks like the investigational medication but does not contain any medicine.
Updated on 19 Feb 2024. Study ID: 1011002931

Interested in the study?

Select a study center that’s convenient for you, and get in touch with the study team.

Connect with the study team