NCT04223427Completed
Effects of Directional Subthalamic Deep Brain Stimulation on Gait and Balance in Parkinson's Disease Patients
Effects of Directional Subthalamic Deep Brain Stimulation on Gait and Balance in Parkinson's Disease Patients - MApping Gait and Balance Issues With Current Shaping
Source: ClinicalTrials.gov · Last updated 6 Feb 2026
Brief summary (registry, in English)
Deep brain stimulation of the NST is effective for cardinal motor signs in patients with idiopathic Parkinson's disease (IPD), its effects on gait disturbances, especially freezing of gait-FOG, and falls are variable from one patient to another, in part depending on the location of the NST-stimulating contact. The ability to change the shape of the current field, and thus the volume of activated tissue, with a directional stimulation electrode is a new treatment option for NSC SCP patients with Parkinson's disease. In this pilot research program, the main objective is to determine the impact of directional DBS on gait and balance issues for PD patients implanted in the STN, using previously described anatomical and functional data for gait disturbances to guide directional programming. Ten patients with Patients with severe form of Parkinson's disease eligible to deep brain stimulation of the subthalamic nucleus, will be included in two French sites.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 19 (actual)
- First submitted
- 10 Dec 2019
- Start date
- 14 Jan 2020
- Primary completion date
- 7 Jul 2025
- Lead sponsor
- University Hospital, Rouen
- Diseases
- Parkinson disease
- NCT number
- NCT04223427
What you commit to
- Study type: Interventional
- Participants enrolled: 19
- From 14 Jan 2020 to the primary completion date, 7 Jul 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Contraindication to research MRI (without contrast product) such as claustrophobia, metallic splinters in the eyes, ferromagnetic foreign bodies close to nerve structures, cardiac, ORL and neurological devices not MRI compatible, wearing of osteosynthseis equipment prior to 1980, metal prostheses, bypass valves ventriculoperitoneal neurosurgery, tattoos containing iron particles…
Other illness
- Actual and severe psychiatric pathology or other neurological disorder
- Dementia (MMS \<24/30)
- Contraindication to surgery: hemostasis trouble, anticoagulants or antiagregants treatment, ongoing infection
- Hypersensitivity to contrasts agents
Age
- Pregnant or parturient or lactating woman or lack of proven and effective contraception according to WHO definition (estrogen-progestin or intra-uterine device or tubal ligation) (for women of childbearing age)
Other
- Persons under guardianship, tutorship or any other administrative or judicial measure of deprivation of rights and liberty
- Subject at the time of exclusion from other biomedical research or participating in any other biomedical research or therapeutic trial
Who the study is looking for
- Age between 18 and 70 years
- Diagnosis of Parkinson's Disease; as defined by the United Kingdom Parkinson's Disease Society Brain Bank (UKPDSBB) criteria
- Patients eligible for subthalamic bilateral deep brain stimulation (STN-DBS) according to local inclusion criteria;
- Freezing of gait in the OFF-dopa condition with item 2.13 of the MDS-UPDRS \> 0 in usual life;
- Patient having read and understood the information letter and signed the Informed Consent Form
- Patient affiliated with, or beneficiary of a social security category
- Stability of others medical disorders or that do not interfere with the research protocol.
- Woman of childbearing potential with effective contraception according to WHO definition (estrogen-progestin or intra-uterine device or tubal ligation) since at least 3 months (negative urinary pregnancy test at inclusion)
Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU de Rouen Coordinator of this site? Confirm its status | Rouen | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.