search
Back to results

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

Primary Purpose

Parkinson Disease

Status
Unknown status
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Kinetra and Soletra (neurostimulator, Medtronic)
Best Medical Treatment
Sponsored by
German Parkinson Study Group (GPS)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson Disease focused on measuring Parkinson Disease, Deep Brain Stimulation, PDQ-39

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Idiopathic Parkinson's Disease Hoehn and Yahr stage ≤ 2.5 in the best "on"med 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

Sites / Locations

  • Michallon Hospital, CHU Grenoble, Service de Neurologie, BP217
  • Service de Neurologie C, Hôpital Neurologique et neurochirurgical Pierre Wertheimer , 59 Bd Pinel 69677 BRON Cedex
  • Centre hospitalier La Timone, Service de neurologie et pathologie du mouvement,Boulevard Jean Moulin
  • "Hôpital Nord Laënnec Boulevard Jacques-Monod - Saint-Herblain
  • CIC, CHU Pitié-Salpêtrière, 47-83 Bd de l'Hôpital
  • Hôpital La Milétrie, Tour Jean Bernard, 350 Av Jacques Cœur, BP 577
  • Centre Hospitalo-Universitaire de Rouen, Charles Nicolle, bat. DV, 1 rue de Germont
  • Centre d'investigation Clinique, Pavillon Riser, Hôpital Purpan,Place du Dr Baylac TSA 40031
  • Klinik und Poliklinik für Neurologie, Charite
  • Neurologische Klinik der Universität, Moorenstr. 5
  • Neurologische Universitätsklinik Freiburg, Breisacher Str. 64
  • Paracelsus-Elena-Klinik, Kassel, Klinikstrasse 16
  • Klinik für Neurologie, Universitätsklinikum Schleswig-Holstein, Schittenhelmstr. 10
  • Klinik und Poliklinik für Neurologie
  • Klinikum der Universität München Neurologische Klinik und Poliklinik - Großhadern, Marchioninistr. 15
  • Universitätsklinikum Tübingen, Klinik für Neurochirurgie, Hoppe-Seyler-Str.3

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

DBS treatment

BMT treatment

Arm Description

Patients in this arm are treated with Deep Brain Stimulation (DBS) of the Nucleus subthalamicus with the device Kinetra and Soletra (neurostimulator, Medtronic) and addtionally get best medical treatment

Patients in this arm get best medical treatment only.

Outcomes

Primary Outcome Measures

PDQ-39
Difference in the PDQ-39 summary index at 24 months compared to the baseline assessment.

Secondary Outcome Measures

UPDRS part III
Change in the Unified Parkinson's disease Rating Scale (UPDRS) part III
UPDRS II scale
Change in the UPDRS II scale
Safety
Frequency, type and severity of therapy related adverse events of medication or DBS, Change in medication (L-DOPA equivalents)
UPDRS VI scale
Change in the UPDRS VI scale
SCOPA-PS
Change in the SCOPA-PS scale
BDI scale
Change in the BDI scale
MADRS scale
Change in the MADRS scale
BPRS scale
Change in the BPRS scale
Mattis Dementia Scale
Change in the Mattis Dementia Scale
Ardouin Behaviour Scale
Change in the Ardouin Behaviour Scale
Starkstein-Apathy Scale
Change in the Starkstein-Apathy Scale
professional Fitness scale
Change in the professional Fitness scale
SF-36 scale
Change in the SF-36 scale
pain (VAS) scale,
Change in the pain (VAS) scale
clinical global impression (CGI-GI) scale
change in the clinical global impression (CGI-GI) scale
"best"-state
Change in the number of hours per day in the "best"-state
"best" state dyskinesias
Frequency and severity of "best" state dyskinesias
Sleeping-hours per day
Sleeping-hours per day
Gait
Changes in gait
Speech
Changes in speech

Full Information

First Posted
July 19, 2006
Last Updated
June 22, 2018
Sponsor
German Parkinson Study Group (GPS)
Collaborators
University Hospital Schleswig-Holstein, Assistance Publique - Hôpitaux de Paris, KKS Netzwerk
search

1. Study Identification

Unique Protocol Identification Number
NCT00354133
Brief Title
Controlled Trial With Deep Brain Stimulation in Patients With Early Parkinson's Disease
Acronym
EARLYSTIM
Official Title
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)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2018
Overall Recruitment Status
Unknown status
Study Start Date
July 2006 (undefined)
Primary Completion Date
March 2022 (Anticipated)
Study Completion Date
March 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
German Parkinson Study Group (GPS)
Collaborators
University Hospital Schleswig-Holstein, Assistance Publique - Hôpitaux de Paris, KKS Netzwerk

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease
Keywords
Parkinson Disease, Deep Brain Stimulation, PDQ-39

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
251 (Actual)

8. Arms, Groups, and Interventions

Arm Title
DBS treatment
Arm Type
Active Comparator
Arm Description
Patients in this arm are treated with Deep Brain Stimulation (DBS) of the Nucleus subthalamicus with the device Kinetra and Soletra (neurostimulator, Medtronic) and addtionally get best medical treatment
Arm Title
BMT treatment
Arm Type
Active Comparator
Arm Description
Patients in this arm get best medical treatment only.
Intervention Type
Device
Intervention Name(s)
Kinetra and Soletra (neurostimulator, Medtronic)
Intervention Description
Patients in this arm were implanted with a neurostimulator (Kinetra and Soletra from Medtronic) are stimulated. Additionally the get best medical treatment.
Intervention Type
Drug
Intervention Name(s)
Best Medical Treatment
Intervention Description
Patients in this arm get best medical treatment only
Primary Outcome Measure Information:
Title
PDQ-39
Description
Difference in the PDQ-39 summary index at 24 months compared to the baseline assessment.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
UPDRS part III
Description
Change in the Unified Parkinson's disease Rating Scale (UPDRS) part III
Time Frame
24 months
Title
UPDRS II scale
Description
Change in the UPDRS II scale
Time Frame
24 months
Title
Safety
Description
Frequency, type and severity of therapy related adverse events of medication or DBS, Change in medication (L-DOPA equivalents)
Time Frame
24 months
Title
UPDRS VI scale
Description
Change in the UPDRS VI scale
Time Frame
24 months
Title
SCOPA-PS
Description
Change in the SCOPA-PS scale
Time Frame
24 months
Title
BDI scale
Description
Change in the BDI scale
Time Frame
24 months
Title
MADRS scale
Description
Change in the MADRS scale
Time Frame
24 months
Title
BPRS scale
Description
Change in the BPRS scale
Time Frame
24 months
Title
Mattis Dementia Scale
Description
Change in the Mattis Dementia Scale
Time Frame
24 months
Title
Ardouin Behaviour Scale
Description
Change in the Ardouin Behaviour Scale
Time Frame
24 months
Title
Starkstein-Apathy Scale
Description
Change in the Starkstein-Apathy Scale
Time Frame
24 months
Title
professional Fitness scale
Description
Change in the professional Fitness scale
Time Frame
24 months
Title
SF-36 scale
Description
Change in the SF-36 scale
Time Frame
24 months
Title
pain (VAS) scale,
Description
Change in the pain (VAS) scale
Time Frame
24 months
Title
clinical global impression (CGI-GI) scale
Description
change in the clinical global impression (CGI-GI) scale
Time Frame
24 months
Title
"best"-state
Description
Change in the number of hours per day in the "best"-state
Time Frame
24 months
Title
"best" state dyskinesias
Description
Frequency and severity of "best" state dyskinesias
Time Frame
24 months
Title
Sleeping-hours per day
Description
Sleeping-hours per day
Time Frame
24 months
Title
Gait
Description
Changes in gait
Time Frame
24 months
Title
Speech
Description
Changes in speech
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Idiopathic Parkinson's Disease Hoehn and Yahr stage ≤ 2.5 in the best "on"med 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guenther Deuschl, Prof.
Organizational Affiliation
Department of Neurology, Christian-Albrechts-University Kiel, Schittenhelmstr. 10, D 24105 Kiel
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marie Vidailhet, Prof.
Organizational Affiliation
Groupe Hospitalier Pitié- Salpêtrière, Fédération des Maladies du Système Nerveux, 47-83 Boulevard de l´Hôpital, F- 75651 Paris Cedex 13
Official's Role
Principal Investigator
Facility Information:
Facility Name
Michallon Hospital, CHU Grenoble, Service de Neurologie, BP217
City
Grenoble Cedex
ZIP/Postal Code
38043
Country
France
Facility Name
Service de Neurologie C, Hôpital Neurologique et neurochirurgical Pierre Wertheimer , 59 Bd Pinel 69677 BRON Cedex
City
Lyon
ZIP/Postal Code
69677
Country
France
Facility Name
Centre hospitalier La Timone, Service de neurologie et pathologie du mouvement,Boulevard Jean Moulin
City
Marseille
ZIP/Postal Code
13005
Country
France
Facility Name
"Hôpital Nord Laënnec Boulevard Jacques-Monod - Saint-Herblain
City
Nantes
ZIP/Postal Code
44093
Country
France
Facility Name
CIC, CHU Pitié-Salpêtrière, 47-83 Bd de l'Hôpital
City
Paris Cedex 13
ZIP/Postal Code
75651
Country
France
Facility Name
Hôpital La Milétrie, Tour Jean Bernard, 350 Av Jacques Cœur, BP 577
City
Poitiers
ZIP/Postal Code
86021
Country
France
Facility Name
Centre Hospitalo-Universitaire de Rouen, Charles Nicolle, bat. DV, 1 rue de Germont
City
Rouen
ZIP/Postal Code
76031
Country
France
Facility Name
Centre d'investigation Clinique, Pavillon Riser, Hôpital Purpan,Place du Dr Baylac TSA 40031
City
Toulouse
ZIP/Postal Code
31059
Country
France
Facility Name
Klinik und Poliklinik für Neurologie, Charite
City
Berlin
Country
Germany
Facility Name
Neurologische Klinik der Universität, Moorenstr. 5
City
Duesseldorf
ZIP/Postal Code
40225
Country
Germany
Facility Name
Neurologische Universitätsklinik Freiburg, Breisacher Str. 64
City
Freiburg
ZIP/Postal Code
79106
Country
Germany
Facility Name
Paracelsus-Elena-Klinik, Kassel, Klinikstrasse 16
City
Kassel
ZIP/Postal Code
34128
Country
Germany
Facility Name
Klinik für Neurologie, Universitätsklinikum Schleswig-Holstein, Schittenhelmstr. 10
City
Kiel
ZIP/Postal Code
24105
Country
Germany
Facility Name
Klinik und Poliklinik für Neurologie
City
Köln
ZIP/Postal Code
50924
Country
Germany
Facility Name
Klinikum der Universität München Neurologische Klinik und Poliklinik - Großhadern, Marchioninistr. 15
City
München
ZIP/Postal Code
81377
Country
Germany
Facility Name
Universitätsklinikum Tübingen, Klinik für Neurochirurgie, Hoppe-Seyler-Str.3
City
Tübingen
ZIP/Postal Code
72076
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results reported in this article, after deidentification (text, tables, figures and appendices).
IPD Sharing Time Frame
Beginning 9 months and ending 36 months following article publication.
IPD Sharing Access Criteria
by inidividual contact with the Coordinatin Investigator Prof.Dr. Deuschl
Citations:
PubMed Identifier
23406026
Citation
Schuepbach WM, Rau J, Knudsen K, Volkmann J, Krack P, Timmermann L, Halbig TD, Hesekamp H, Navarro SM, Meier N, Falk D, Mehdorn M, Paschen S, Maarouf M, Barbe MT, Fink GR, Kupsch A, Gruber D, Schneider GH, Seigneuret E, Kistner A, Chaynes P, Ory-Magne F, Brefel Courbon C, Vesper J, Schnitzler A, Wojtecki L, Houeto JL, Bataille B, Maltete D, Damier P, Raoul S, Sixel-Doering F, Hellwig D, Gharabaghi A, Kruger R, Pinsker MO, Amtage F, Regis JM, Witjas T, Thobois S, Mertens P, Kloss M, Hartmann A, Oertel WH, Post B, Speelman H, Agid Y, Schade-Brittinger C, Deuschl G; EARLYSTIM Study Group. Neurostimulation for Parkinson's disease with early motor complications. N Engl J Med. 2013 Feb 14;368(7):610-22. doi: 10.1056/NEJMoa1205158.
Results Reference
result
PubMed Identifier
23697520
Citation
Deuschl G, Schade-Brittinger C, Agid Y; EARLYSTIM Study Group. Neurostimulation for Parkinson's disease with early motor complications. N Engl J Med. 2013 May 23;368(21):2038. doi: 10.1056/NEJMc1303485. No abstract available.
Results Reference
result
PubMed Identifier
27506638
Citation
Dams J, Balzer-Geldsetzer M, Siebert U, Deuschl G, Schuepbach WM, Krack P, Timmermann L, Schnitzler A, Reese JP, Dodel R; EARLYSTIM-investigators. Cost-effectiveness of neurostimulation in Parkinson's disease with early motor complications. Mov Disord. 2016 Aug;31(8):1183-91. doi: 10.1002/mds.26740.
Results Reference
result
PubMed Identifier
29452685
Citation
Lhommee E, Wojtecki L, Czernecki V, Witt K, Maier F, Tonder L, Timmermann L, Halbig TD, Pineau F, Durif F, Witjas T, Pinsker M, Mehdorn M, Sixel-Doring F, Kupsch A, Kruger R, Elben S, Chabardes S, Thobois S, Brefel-Courbon C, Ory-Magne F, Regis JM, Maltete D, Sauvaget A, Rau J, Schnitzler A, Schupbach M, Schade-Brittinger C, Deuschl G, Houeto JL, Krack P; EARLYSTIM study group. Behavioural outcomes of subthalamic stimulation and medical therapy versus medical therapy alone for Parkinson's disease with early motor complications (EARLYSTIM trial): secondary analysis of an open-label randomised trial. Lancet Neurol. 2018 Mar;17(3):223-231. doi: 10.1016/S1474-4422(18)30035-8.
Results Reference
result
PubMed Identifier
25399678
Citation
Schupbach WM, Rau J, Houeto JL, Krack P, Schnitzler A, Schade-Brittinger C, Timmermann L, Deuschl G. Myths and facts about the EARLYSTIM study. Mov Disord. 2014 Dec;29(14):1742-50. doi: 10.1002/mds.26080. Epub 2014 Nov 14.
Results Reference
result
PubMed Identifier
22841616
Citation
Deuschl G, Schupbach M, Knudsen K, Pinsker MO, Cornu P, Rau J, Agid Y, Schade-Brittinger C. Stimulation of the subthalamic nucleus at an earlier disease stage of Parkinson's disease: concept and standards of the EARLYSTIM-study. Parkinsonism Relat Disord. 2013 Jan;19(1):56-61. doi: 10.1016/j.parkreldis.2012.07.004. Epub 2012 Jul 28.
Results Reference
result
PubMed Identifier
30737338
Citation
Schuepbach WMM, Tonder L, Schnitzler A, Krack P, Rau J, Hartmann A, Halbig TD, Pineau F, Falk A, Paschen L, Paschen S, Volkmann J, Dafsari HS, Barbe MT, Fink GR, Kuhn A, Kupsch A, Schneider GH, Seigneuret E, Fraix V, Kistner A, Chaynes PP, Ory-Magne F, Brefel-Courbon C, Vesper J, Wojtecki L, Derrey S, Maltete D, Damier P, Derkinderen P, Sixel-Doring F, Trenkwalder C, Gharabaghi A, Wachter T, Weiss D, Pinsker MO, Regis JM, Witjas T, Thobois S, Mertens P, Knudsen K, Schade-Brittinger C, Houeto JL, Agid Y, Vidailhet M, Timmermann L, Deuschl G; EARLYSTIM study group. Quality of life predicts outcome of deep brain stimulation in early Parkinson disease. Neurology. 2019 Mar 5;92(10):e1109-e1120. doi: 10.1212/WNL.0000000000007037. Epub 2019 Feb 8. Erratum In: Neurology. 2019 Jun 11;92(24):1166.
Results Reference
derived
Links:
URL
http://www.kompetenznetz-parkinson.de/
Description
(German Research Collaboration, funded by the German Ministry of Research)
URL
http://www.kks.uni-marburg.de/
Description
(Homepage Coordination Center for Clinical Studies to STN Study, Language: German)
URL
http://www.kks.uni-marburg.de/
Description
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.

Learn more about this trial

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

We'll reach out to this number within 24 hrs