Skip to content

Controlled Trial With Deep Brain Stimulation in Patients With Early Parkinson's Disease

The Effect of Deep Brain Stimulation of the Subthalamic Nucleus (STN-DBS) on Quality of Life in Comparison to Best Medical Treatment in Patients With Complicated Parkinson's Disease and Preserved Psychosocial Competence (EARLYSTIM-study)

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00354133
Acronym
EARLYSTIM
Enrollment
251
Registered
2006-07-20
Start date
2006-07-31
Completion date
2022-03-31
Last updated
2018-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson Disease

Keywords

Parkinson Disease, Deep Brain Stimulation, PDQ-39

Brief summary

Earlystim Study: Patients are randomized either to medical treatment or subthalamic stimulation. The observation period was 2 years. The primary outcome criterium: PDQ-39. Post study Follow up studies: After the 24 months observation period also BMT patients could be operated and all patients will be observed for 10 years or longer to elucidate whether earlier stimulation has advantages (or drawbacks) compared to later stimulation.

Detailed description

Parkinsons' disease is one of the most disabling chronic neurological diseases. It can be treated sufficiently until motor complications with fluctuations of mobility and dyskinesias develop. The quality of life and the social and occupational functioning is relentlessly deteriorating with longer disease duration once the complications of conservative therapy develop. High-frequency stimulation of the subthalamic nucleus especially improves the motor complications of Parkinson's disease and preliminary data suggest that also the quality of life and psychosocial handicap are improved. So far this therapy is only used for patients which have already undergone personal, professional and social degradation due to motor complications of the disease. The aim of this study is to assess the use of this therapy in earlier stages of the disease, when motor complications have just developed and before patients are significantly affected in their social and occupational functioning. The main study (Earlystim) was finished in March 2012 and published in February 2013 (Schuepbach WM, Rau J, Knudsen K, et al. Neurostimulation for Parkinson's disease with early motor complications. N Engl J Med. Feb 14 2013;368(7):610-622.) Patients, who were treated with BMT only in the Earlystim Study were privileged to be operated after the 24 months and a follow up phase of 5 years was planned to elucidate whether earlier stimulation has advantages (or drawbacks) compared to later stimulation. As operated patients fare better in terms of quality of life and other outcomes (see publication), it will be important to know if patients who are operated earlier keep an advantage in all thoses parameters over those who were operated later or if those operated later will catch up after surgery. Also the pattern of adverse events among earlier and later operated patients may differ. These issues can be addressed with the post-study follow-up (PSFU) studies of the patients of the Earlystim trial. The results of these investigations elucidate longterm issues of DBS in PD and may affect the recommendations of surgery for patients.

Interventions

DRUGBest Medical Treatment

Patients in this arm get best medical treatment only

DEVICEKinetra and Soletra (neurostimulator, Medtronic)

Patients in this arm were implanted with a neurostimulator (Kinetra and Soletra from Medtronic) are stimulated. Additionally the get best medical treatment.

Sponsors

University Hospital Schleswig-Holstein
CollaboratorOTHER
Assistance Publique - Hôpitaux de Paris
CollaboratorOTHER
KKS Netzwerk
CollaboratorNETWORK
German Parkinson Study Group (GPS)
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Idiopathic Parkinson's Disease * Hoehn and Yahr stage ≤ 2.5 in the best onmed condition * Disease duration \> 4 years * Presence of fluctuations and/or dyskinesias for no more than 3 years * One of the two following forms of impairment: * Impairment in activities of daily living (UPDRS II \> 6) due to PD-symptoms despite medical treatment in the worst condition or * Impairment of social and occupational functioning (measured with a modified SOFAS) due to PD-symptoms despite medical treatment (51-80%) * PDQ-39 completed * Written informed consent * For the patients in France a social security number is required

Exclusion criteria

* Major depression with suicidal thoughts (Beck Depression Inventory \> 25) * Dementia (Mattis Score ≤ 130) * Acute psychosis * Need for nursing care * Any medical or psychological problems which may interfere with a smooth conduction of the study protocol (e.g. cancer with a limited life expectancy) * Drug or alcohol addiction * Surgical contraindications * Fertile women not using adequate contraceptive methods * Women who are pregnant or breast feeding * Illiteracy or insufficient language skills (German or French) to complete the questionnaires * Simultaneous participation in another clinical trial except that other trial does not affect the Earlystim study as approved and documented by the steering committee

Design outcomes

Primary

MeasureTime frameDescription
PDQ-3924 monthsDifference in the PDQ-39 summary index at 24 months compared to the baseline assessment.

Secondary

MeasureTime frameDescription
professional Fitness scale24 monthsChange in the professional Fitness scale
SF-36 scale24 monthsChange in the SF-36 scale
pain (VAS) scale,24 monthsChange in the pain (VAS) scale
clinical global impression (CGI-GI) scale24 monthschange in the clinical global impression (CGI-GI) scale
best-state24 monthsChange in the number of hours per day in the best-state
best state dyskinesias24 monthsFrequency and severity of best state dyskinesias
Sleeping-hours per day24 monthsSleeping-hours per day
Gait24 monthsChanges in gait
Speech24 monthsChanges in speech
Starkstein-Apathy Scale24 monthsChange in the Starkstein-Apathy Scale
Mattis Dementia Scale24 monthsChange in the Mattis Dementia Scale
Ardouin Behaviour Scale24 monthsChange in the Ardouin Behaviour Scale
UPDRS part III24 monthsChange in the Unified Parkinson's disease Rating Scale (UPDRS) part III
UPDRS II scale24 monthsChange in the UPDRS II scale
Safety24 monthsFrequency, type and severity of therapy related adverse events of medication or DBS, Change in medication (L-DOPA equivalents)
UPDRS VI scale24 monthsChange in the UPDRS VI scale
SCOPA-PS24 monthsChange in the SCOPA-PS scale
BDI scale24 monthsChange in the BDI scale
MADRS scale24 monthsChange in the MADRS scale
BPRS scale24 monthsChange in the BPRS scale

Countries

France, Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026