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.
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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
251
Patients in this arm were implanted with a neurostimulator (Kinetra and Soletra from Medtronic) are stimulated. Additionally the get best medical treatment.
Patients in this arm get best medical treatment only
Michallon Hospital, CHU Grenoble, Service de Neurologie, BP217
Grenoble, France
Service de Neurologie C, Hôpital Neurologique et neurochirurgical Pierre Wertheimer , 59 Bd Pinel 69677 BRON Cedex
PDQ-39
Difference in the PDQ-39 summary index at 24 months compared to the baseline assessment.
Time frame: 24 months
UPDRS part III
Change in the Unified Parkinson's disease Rating Scale (UPDRS) part III
Time frame: 24 months
UPDRS II scale
Change in the UPDRS II scale
Time frame: 24 months
Safety
Frequency, type and severity of therapy related adverse events of medication or DBS, Change in medication (L-DOPA equivalents)
Time frame: 24 months
UPDRS VI scale
Change in the UPDRS VI scale
Time frame: 24 months
SCOPA-PS
Change in the SCOPA-PS scale
Time frame: 24 months
BDI scale
Change in the BDI scale
Time frame: 24 months
MADRS scale
Change in the MADRS scale
Time frame: 24 months
BPRS scale
Change in the BPRS scale
Time frame: 24 months
Mattis Dementia Scale
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Lyon, France
Centre hospitalier La Timone, Service de neurologie et pathologie du mouvement,Boulevard Jean Moulin
Marseille, France
"Hôpital Nord Laënnec Boulevard Jacques-Monod - Saint-Herblain
Nantes, France
CIC, CHU Pitié-Salpêtrière, 47-83 Bd de l'Hôpital
Paris, France
Hôpital La Milétrie, Tour Jean Bernard, 350 Av Jacques Cœur, BP 577
Poitiers, France
Centre Hospitalo-Universitaire de Rouen, Charles Nicolle, bat. DV, 1 rue de Germont
Rouen, France
Centre d'investigation Clinique, Pavillon Riser, Hôpital Purpan,Place du Dr Baylac TSA 40031
Toulouse, France
Klinik und Poliklinik für Neurologie, Charite
Berlin, Germany
Klinik und Poliklinik für Neurologie
Cologne, Germany
...and 6 more locations
Change in the Mattis Dementia Scale
Time frame: 24 months
Ardouin Behaviour Scale
Change in the Ardouin Behaviour Scale
Time frame: 24 months
Starkstein-Apathy Scale
Change in the Starkstein-Apathy Scale
Time frame: 24 months
professional Fitness scale
Change in the professional Fitness scale
Time frame: 24 months
SF-36 scale
Change in the SF-36 scale
Time frame: 24 months
pain (VAS) scale,
Change in the pain (VAS) scale
Time frame: 24 months
clinical global impression (CGI-GI) scale
change in the clinical global impression (CGI-GI) scale
Time frame: 24 months
"best"-state
Change in the number of hours per day in the "best"-state
Time frame: 24 months
"best" state dyskinesias
Frequency and severity of "best" state dyskinesias
Time frame: 24 months
Sleeping-hours per day
Sleeping-hours per day
Time frame: 24 months
Gait
Changes in gait
Time frame: 24 months
Speech
Changes in speech
Time frame: 24 months