NCT06498349Recruiting
Bilateral Subthalamic Stimulation in PD Patients With Impulse Control Disorders - STIMPulseControl
A Randomized Controlled Trial of Bilateral Subthalamic Stimulation in Patients With Parkinson's Disease and Impulse Control Disorders
Source: ClinicalTrials.gov · Last updated 20 Oct 2026
Brief summary (registry, in English)
The focus of the study is on patients Parkinson's disease showing as well behavioral disorders that can be described as pathological and are summarized under the term impulse control disorder (ICD). Changes in behavior and also pathological disorders are a common side effect of treatment for Parkinson's disease. The goal of this academic study is to compare the effect of surgical (deep brain stimulation, DBS) treatment combined with a coordinated and adapted best medical treatment (BMT) to be compared with the effect of optimized best medical treatment (BMT) alone. The stimulation arm (DBS+BMT) as well as the medication arm (BMT only) will be monitored according to clinical routine. Participants will have to agree to be randomly assigned to either deep brain stimulation in combination with the best medical treatment (DBS group) or the best medical treatment alone (BMT group). Participants will have to come regularly according to clinical routine to the clinic and complete various questionaires and scales for the study.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- First submitted
- 17 Jun 2024
- Start date
- 5 Sept 2024
- Primary completion date
- 15 Jul 2027
- Lead sponsor
- University of Kiel
- Diseases
- Parkinson disease
- NCT number
- NCT06498349
What you commit to
- Study type: Interventional
- Planned participants: 60
- From 5 Sept 2024 to the primary completion date, 15 Jul 2027
- 13 sites in 3 countries
- 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
- Surgical contraindications to undergo DBS operation
- Any prior movement disorder treatments that involved intracranial surgery/ablation or intracranial device implantation
Other illness
- Dementia (MoCA \< 24) in the meds on condition
- Any history of recurrent seizures or haemorrhagic stroke
- Any terminal illness with significantly reduced life expectancy which exclude DBS implantation according to standard clinical care
- Any impairment that would limit subject's ability to participate in the study and perform study procedures
- Have any significant medical condition that is likely to interfere with study procedures or likely to confound evaluation of study endpoints
Other
- Ongoing severe depression (BDI-II \> 28)
- suicidal ideation (item 9 of BDI-II \> 1)
- Any other active implanted device that is likely to interfere with the implantation or functioning of the DBS system
- Simultaneous participation in another clinical trial targeting or potentially interfering with ICD
- Fertile women not using adequate contraceptive methods
- A female who is breastfeeding or of child-bearing potential with a positive urine pregnancy test or not using adequate contraception
Who the study is looking for
- Age at the time of enrollment: ≤ 70 years
- Diagnosis of PD according to MDS clinical diagnostic criteria
- Onset of first PD motor symptoms ≥ 4 years
- Moderate or severe impulse control disorder or related behavioral disorders according to Ardouin, with at least 1 score greater than or equal to 3 (or at least 2 scores greater than or equal to 2) on the Ardouin behaviour scale with the following items considered to reflect ICBDs or related behaviors: pathological gambling, hypersexuality, shopping, eating, hobbyism, punding and compulsive medication use
- MDS-UPDRS III improvement of ≥ 30% in the standardized levodopa test or classical Parkinsonian tremor at rest
- Adaptation of medical therapy has been attempted
- MoCA ≥ 24 in the meds on condition
- BDI-II score \< 20 in the meds on condition, or Patients with moderately severe depression with a BDI-II between 20 and 28 points, strict consideration must be made with the involvement of a psychiatrist. Patients must be willing and able to comply this.
- Patients able to understand the study requirements and the treatment procedures
- Written informed consent before any study-specific tests or procedures are performed
Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers
Sites (13)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Hospital of Bern (Inselspital) Coordinator of this site? Confirm its status | Bern | Switzerland | Recruiting |
| University Hospital Zuerich (USZ) Coordinator of this site? Confirm its status | Zurich | Switzerland | Recruiting |
| University Hospital Cologne Coordinator of this site? Confirm its status | Cologne | Germany | Recruiting |
| University Hospital Carl Gustav Carus Coordinator of this site? Confirm its status | Dresden | Germany | Recruiting |
| University Hospital Duesseldorf Coordinator of this site? Confirm its status | Düsseldorf | Germany | Recruiting |
| University Medical Center Hamburg-Eppendorf Coordinator of this site? Confirm its status | Hamburg | Germany | Recruiting |
| Paracelsus - Elena- Klinik Coordinator of this site? Confirm its status | Kassel | Germany | Not yet recruiting |
| University Hospital Schleswig-Holstein (UKSH), Campus Kiel Coordinator of this site? Confirm its status | Kiel | Germany | Recruiting |
| University Hospital of Giessen and Marburg (UKGM), Campus Marburg Coordinator of this site? Confirm its status | Marburg | Germany | Recruiting |
| Charité Campus Mitte Coordinator of this site? Confirm its status | Mitte | Germany | Recruiting |
| University Hospital Tuebingen Coordinator of this site? Confirm its status | Tübingen | Germany | Recruiting |
| University Hospital Wuerzburg Coordinator of this site? Confirm its status | Würzburg | Germany | Recruiting |
| Amsterdam University Medical Center Coordinator of this site? Confirm its status | Amsterdam | Netherlands | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.