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Clinical Trials/NCT04524377
NCT04524377
Unknown
Not Applicable

Evaluation of the Influence of Deep Brain Stimulation on the Spinal Deformities Associated With Parkinson's Disease

Charite University, Berlin, Germany1 site in 1 country47 target enrollmentJuly 25, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parkinson Disease
Sponsor
Charite University, Berlin, Germany
Enrollment
47
Locations
1
Primary Endpoint
Sagittal Imbalance
Last Updated
5 years ago

Overview

Brief Summary

The intention of the study is to investigate whether Deep Brain Stimulation (DBS) will improve postural deformities of patients with Parkinson's disease.

Detailed Description

1. Introduction Postural deformities are frequent comorbidities that limit the quality of life in patients with Parkinson's disease. Subject of the study is the investigation of postural deformities as a concomitant disease in connection with therapy with DBS. The aim of this prospective study is to examine the effect of deep brain stimulation on postural instability and thus the quality of life of patients. 2. Study outline The aim of this prospective study is to investigate the effect of DBS on postural instability and thus the quality of life of patients. For this purpose, the investigators would like to evaluate 50 participants before and at certain time points (three, six, twelve and 24 months) after DBS surgery. X-rays of the entire spine are carried out using EOS® technology and biodynamic measurements of the spine using the Epionics SPINE ® system. In addition, the Investigators collect the 39-item PD Questionnaires (PDQ-39), Unified Parkinson's Disease Rating Scale (UPDRS) Part III, Visual Analog Scale (VAS) and Oswestry Disability Index (ODI) as clinical parameters. Our hypotheses (I): DBS improves the sagittal balance of the spine and the pelvic rotation as a corresponding compensation mechanism for this incorrect posture (II) The participant's mobility improves in course of DBS in terms of scope and speed (III) In course after DBS, back pain is significantly reduced and the participant's everyday life is easier to cope with. The investigators hope to gain new insights into the pathophysiology of the spinal deformities associated with Parkinson's disease from the study and to expand the indication for DBS to include clinically relevant spinal complaints. 3. Consent to the study The study was positively assessed by the Charité ethics committee and the Federal Office for Radiation Protection. Consent for study inclusion is sought after explanation and agreement to DBS treatment for participants with Parkinson's disease. Thus, participants capable of consenting to the DBS treatment get the study details explained themselves and may or may not agree to participate. If a participant is incapable for consenting to the proposed treatment, he may not be enrolled in the study. 4. Safety of DBS for Parkinson's disease and further risks for participants Deep brain stimulation is a well-established and well-tolerated treatment for Parkinson's disease. The study-related risks result from the multiple X-ray examinations of the spine (effective dose 2.6 µSv per examination). There are no other study-related risks of the planned ones. 5. Insurance Coverage An insurance was taken out for all study participants who took part in this study at HDI-Gerling Industrie Versichung AG, Riethorst 2, 30659 Hanover, Insurance number: 5701032603017. German laws §§ 40 to 42 Arzneimittelgesetz or §§ 20 to 23 Medizinproduktegesetz are not applicable. The Investigators are insured against fault-based damage through the existing liability insurance of their clinic.

Registry
clinicaltrials.gov
Start Date
July 25, 2019
End Date
September 30, 2023
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Philipp Spindler

Dr. med. Philipp Spindler, Resident, Principal Investigator, Charite University medicine / department of neurosurgery

Charite University, Berlin, Germany

Eligibility Criteria

Inclusion Criteria

  • women and men, over 18 years of age
  • medical indication for deep brain Stimulation for Parkinson's Disease
  • signed declaration of consent

Exclusion Criteria

  • withdrawal of consent
  • non-Parkinson's-associated diseases of the spine
  • pregnancy

Outcomes

Primary Outcomes

Sagittal Imbalance

Time Frame: Two years after DBS

Sagittal vertical axis (SVA) in X-Ray of the Spine. SVA is identified as the location of the head with respect to the normal center of gravity by a plumb line dropped from the center of the C7 vertebral body to the posterior superior corner of the sacral end plate. It is measured in cm with pathological values \>5cm and sagital Imbalance defined as SVA \>10cm.

Secondary Outcomes

  • Pelvic incidence (PI)(Two years after DBS)
  • Spine Mobility(Two years after DBS)
  • Unified Parkinsons Disease Rating Scala (Part III Motor Examination) (UPDRS-Part III)(Two years after DBS)
  • Visual Analoge Scale (VAS)(Two years after DBS)
  • Sacral slope (SS)(Two years after DBS)
  • Oswestry Disability Index (ODI)(Two years after DBS)
  • Scoliosis(Two years after DBS)
  • Parkinsons Disease Questionaire 39 (PDQ-39)(Two years after DBS)
  • Pelvit tilt (PT)(Two years after DBS)
  • Lumbar Lordisis (LL)(Two years after DBS)
  • Mismatch of Pelvic incidence and LL (PI - LL)(Two years after DBS)

Study Sites (1)

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