Could your own nerves help treat Parkinson's? early trial tests idea
NCT ID NCT02369003
First seen Jun 25, 2026 · Last updated Sep 01, 2026 · Updated 3 times
Summary
This study is testing whether implanting a small piece of a patient's own nerve tissue into the brain during deep brain stimulation (DBS) surgery is safe and doable for people with Parkinson's disease. The nerve tissue contains cells that produce growth factors, which might help protect brain cells. The trial involves 70 participants and focuses on safety and side effects, not yet on whether it improves symptoms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- autologous peripheral nerve graft (patient's own nerve tissue)
- What this could lead to
- If successful, this could point toward a new way to support brain cells and slow Parkinson's progression alongside standard DBS treatment.
- What could go wrong
- This is a very early, small pilot study focused on safety, not effectiveness. The nerve graft may not provide any benefit, and surgery carries risks like infection or bleeding.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
-
70 people
The number who actually took part.
- Started
-
Feb 2015
- Expected to finish
-
Sep 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
40 to 75 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Undergoing DBS of the STN or GPi * Between the ages of 40-75 * Able to give informed consent * Show a positive response to Sinemet (carbidopa/levodopa) * Be able to tolerate the surgical procedure Exclusion Criteria: * Any condition that would not make the subject a candidate for DBS of the STN or GPi * Under the age of 40 or over the age of 75 * Unable to give informed consent * Female who is pregnant, lactating, or of child-bearing potential unwilling to use an adequate birth control method during the period of the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Kentucky
Lexington, Kentucky, 40536, United States
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Other studies related to the condition(s) this trial covers.
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