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Efficacy and Safety of DBS in Patients With Primary Dystonia

Primary Purpose

Dystonia

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Beijing Pins Medical Co., Ltd. Deep Brain Stimulator
Sponsored by
Beijing Pins Medical Co., Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dystonia

Eligibility Criteria

6 Years - 60 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Refractory primary (systemic, segmental) dystonia diagnosed by a movement disorders neurologist
  2. Severe functional impairment despite optimal medical management, including failed botulinum toxin therapy
  3. Ability to follow up with post-operative study visits
  4. Patients and their relatives have reasonable surgery expectations
  5. Volunteer to participate in clinical trials, and signed consent form
  6. Age 6-60 years

Exclusion Criteria:

  1. Pregnancy or plan a pregnancy
  2. Good treatment with Non-invasive therapy
  3. Dopamine reactive dystonia ,Genetic degeneration ,Paroxysmal dystonia ,Secondary dystonia, Psychogenic dystonia
  4. Brain MRI showing extensive brain atrophy or small vessel ischemic disease
  5. Cognitive impairment(MMSE<24)
  6. Severe depression or other serious mental illness
  7. History of traumatic brain injury, tumor, or severe cerebrovascular disease
  8. Severe brain atrophy (diagnosed by CT or MRI)
  9. Hyperthermia therapy in implant parts
  10. Abnormal in blood inspection, blood clotting disorders, liver and kidney dysfunction, or other clinical judgment cannot tolerate surgery
  11. High blood pressure, serious heart diseases, or respiratory diseases
  12. Diabetes
  13. Long-term treatment of immunosuppressive or hormones
  14. Implant pacemakers, defibrillators, cochlear and other nerve stimulators
  15. Other diseases need frequent MRI examinations
  16. Participated in any other clinical trials within 3 months
  17. Reluctant or unable to implant surgery
  18. Reluctant or unable to cooperate with follow-up
  19. Other exclusion Criteria by researchers

Sites / Locations

  • Beijing Union Medical College Hospital
  • Union Hospital Tongji Medical College Huazhong University of Science and Technology
  • Nanjing Brain Hospital
  • Qilu Hospital of Shandong University
  • Tongji Hospital of Tongji Univeristy
  • West China Hospital Sichuan University
  • Sir Run Run Shaw Hospital,School of Medicine,Zhejiang University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

STN

GPi

Arm Description

DBS target with Subthalamic Nucleus (STN).

DBS target with Globus Pallidus Internus (GPi).

Outcomes

Primary Outcome Measures

change in Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS) movement score

Secondary Outcome Measures

Short-Form General Health Survey (SF-36)
Quality of life was assessed with the Medical Outcomes Study 36-item Short-Form General Health Survey (SF-36), which evaluates both physical and mental components of functioning on a scale of 0 to 100, with higher scores indicating a higher level of function.
Visual analogue scale
The severity of dystonia and pain was assessed with the use of a visual analogue scale, with scores ranging from 0 to 10 and higher scores indicating greater severity
Measurements of walking
Measurements of walking (the duration and number of steps taken in a 14-m walk with one turn)
The Beck Depression Inventory
The Beck Depression Inventory (with scores ranging from 0 to 63 and higher scores indicating more severe depression)
Mini-Mental State Examination
Cognitive were assessed by mini-mental state examination
The rate of improvement of BFMDRS score
The rate of improvement of BFMDRS score that >25%、>50%、>75%

Full Information

First Posted
January 5, 2017
Last Updated
July 12, 2023
Sponsor
Beijing Pins Medical Co., Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT03017586
Brief Title
Efficacy and Safety of DBS in Patients With Primary Dystonia
Official Title
Subthalamic Nucleus (STN) and Globus Pallidus Internus (GPi) Deep Brain Stimulation (DBS) in Patients With Primary Dystonia(RELAX Study)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
December 27, 2017 (Actual)
Primary Completion Date
September 13, 2020 (Actual)
Study Completion Date
December 17, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Beijing Pins Medical Co., Ltd

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the safety and effectiveness of deep brain stimulation (DBS) of the subthalamic nucleus (STN) and globus pallidus internus (GPi) for primary dystonia.
Detailed Description
Dystonia is an uncommon brain disorder in which there is abnormal muscle tone producing twisting, writhing movements and abnormal postures. It is associated with abnormal electrical activity in two groups of nerve cells in the brain called the globus pallidus internus (GPi) and the subthalamic nucleus (STN). GPi DBS appears to be effective for medication-refractory focal and segmental dystonia affecting the cranial and cervical regions in open-label series, but recently GPi stimulation has been associated with subtle motor disturbances in previously non-dystonic body regions (i.e., arms and legs) in this population of patients. DBS of the STN has also been reported to be effective for treating generalized and cervical dystonia in small open label trials. STN DBS for cranial and cervical regions may provide similar efficacy in the treatment of dystonia as GPi DBS, but without unwanted stimulation-induced motor effects. Objectives of this study is to evaluate the safety and efficacy of STN-DBS and GPi-DBS for dystonia; Participants will be evaluated pre- and postoperatively with standard dystonia rating scales including the Burke-Fahn-Marsden Dystonia rating scale (BFMDRS), Changes in cognitive function will be assessed with neuropsychological testing. Stimulation parameters will be documented, and a patient questionnaire will be administered postoperatively to determine if patients are experiencing stimulation-induced motor adverse effects. Patient weight will be recorded at study visits. This pilot study will provide preliminary open label efficacy outcomes for STN DBS in the treatment of primary dystonia and will help determine if this target should be compared to GPi DBS in a larger double-blind trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dystonia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
69 (Actual)

8. Arms, Groups, and Interventions

Arm Title
STN
Arm Type
Experimental
Arm Description
DBS target with Subthalamic Nucleus (STN).
Arm Title
GPi
Arm Type
Experimental
Arm Description
DBS target with Globus Pallidus Internus (GPi).
Intervention Type
Device
Intervention Name(s)
Beijing Pins Medical Co., Ltd. Deep Brain Stimulator
Intervention Description
Deep Brain Stimulation for primary dystonia subjects
Primary Outcome Measure Information:
Title
change in Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS) movement score
Time Frame
3,6 months
Secondary Outcome Measure Information:
Title
Short-Form General Health Survey (SF-36)
Description
Quality of life was assessed with the Medical Outcomes Study 36-item Short-Form General Health Survey (SF-36), which evaluates both physical and mental components of functioning on a scale of 0 to 100, with higher scores indicating a higher level of function.
Time Frame
3,6 monthsthe Beck Anxiety Inventory31 (with scores ranging from 0 to 63 and higher scores indicating more severe anxiety)
Title
Visual analogue scale
Description
The severity of dystonia and pain was assessed with the use of a visual analogue scale, with scores ranging from 0 to 10 and higher scores indicating greater severity
Time Frame
3,6 months
Title
Measurements of walking
Description
Measurements of walking (the duration and number of steps taken in a 14-m walk with one turn)
Time Frame
3,6 months
Title
The Beck Depression Inventory
Description
The Beck Depression Inventory (with scores ranging from 0 to 63 and higher scores indicating more severe depression)
Time Frame
3,6 months
Title
Mini-Mental State Examination
Description
Cognitive were assessed by mini-mental state examination
Time Frame
3,6 months
Title
The rate of improvement of BFMDRS score
Description
The rate of improvement of BFMDRS score that >25%、>50%、>75%
Time Frame
3,6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Refractory primary (systemic, segmental) dystonia diagnosed by a movement disorders neurologist Severe functional impairment despite optimal medical management, including failed botulinum toxin therapy Ability to follow up with post-operative study visits Patients and their relatives have reasonable surgery expectations Volunteer to participate in clinical trials, and signed consent form Age 6-60 years Exclusion Criteria: Pregnancy or plan a pregnancy Good treatment with Non-invasive therapy Dopamine reactive dystonia ,Genetic degeneration ,Paroxysmal dystonia ,Secondary dystonia, Psychogenic dystonia Brain MRI showing extensive brain atrophy or small vessel ischemic disease Cognitive impairment(MMSE<24) Severe depression or other serious mental illness History of traumatic brain injury, tumor, or severe cerebrovascular disease Severe brain atrophy (diagnosed by CT or MRI) Hyperthermia therapy in implant parts Abnormal in blood inspection, blood clotting disorders, liver and kidney dysfunction, or other clinical judgment cannot tolerate surgery High blood pressure, serious heart diseases, or respiratory diseases Diabetes Long-term treatment of immunosuppressive or hormones Implant pacemakers, defibrillators, cochlear and other nerve stimulators Other diseases need frequent MRI examinations Participated in any other clinical trials within 3 months Reluctant or unable to implant surgery Reluctant or unable to cooperate with follow-up Other exclusion Criteria by researchers
Facility Information:
Facility Name
Beijing Union Medical College Hospital
City
Beijing
State/Province
Beijing
Country
China
Facility Name
Union Hospital Tongji Medical College Huazhong University of Science and Technology
City
Wuhan
State/Province
Hubei
Country
China
Facility Name
Nanjing Brain Hospital
City
Nanjing
State/Province
Jiangsu
Country
China
Facility Name
Qilu Hospital of Shandong University
City
Jinan
State/Province
Shandong
Country
China
Facility Name
Tongji Hospital of Tongji Univeristy
City
Shanghai
State/Province
Shanghai
Country
China
Facility Name
West China Hospital Sichuan University
City
Chengdu
State/Province
Sichuan
Country
China
Facility Name
Sir Run Run Shaw Hospital,School of Medicine,Zhejiang University
City
Hangzhou
State/Province
Zhejiang
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data is available upon request.
IPD Sharing Time Frame
De-identified data may be available after results have been published
IPD Sharing Access Criteria
Individual participant data is available upon request.
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Efficacy and Safety of DBS in Patients With Primary Dystonia

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