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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02601144
Other study ID # PINS-014
Secondary ID
Status Completed
Phase Phase 1
First received October 12, 2015
Last updated March 18, 2017
Start date October 2015
Est. completion date December 2016

Study information

Verified date March 2017
Source Beijing Pins Medical Co., Ltd
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is the first study on the effect of the variable frequency stimulation (VFS) on Freezing of gait (FOG) in Parkinson's disease (PD) patients with STN DBS. FOG has responded poorly to High frequency stimulation (HFS) but can be alleviated by relatively VFS. This study would have significant clinical implications in the management of Freezing of gait (FOG) in these PD patients with subthalamic nucleus (STN) DBS. The investigators hypothesize that VFS could have better effect on FOG than HFS and low frequency stimulation (LFS).


Description:

HFS of STN provides consistent, long-term improvement of the cardinal motor signs of PD, such as bradykinesia, tremor and rigidity. FOG has responded poorly to HFS and tends to continue to deteriorate over time, but this can be alleviated by relatively LFS. Evidence has indicated that LFS-STN can improve axial signs in some but not all PD patients, but most of them experienced loss of efficacy in the short term. Then comes to the little improvement or even worse of tremor, rigidity and bradykinesia, which consists of the three main symptoms of Parkinson's disease. Thus even if axial problems could be solved by LFS in a long way, it could also be hard to tolerate by those patients. The effect of VFS on FOG will be studied. The investigators hypothesize that VFS could have better effect on Freezing of gait than HFS and LFS.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Patients were receiving bilateral STN stimulation for more than six months.

2. They were optimized on conventional HFS for control of tremors, rigidity and bradykinesia yet complained of freezing of gait.

3. Subjects had an ability to walk at least 10 meters independently during ON DBS condition.

Exclusion criteria:

1. gait disorders perceived by patients as a direct consequence of STN stimulation and not the primary disease.

2. any change in the HFS DBS settings, three months prior to participation in the study.

3. complete inability to walk despite assistance while DBS ON.

4. Subjects responding to reprogramming of chronic DBS settings (report improvement of freezing).

5. Subjects could not tolerate prolonged OFF medication condition.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Deep Brain Stimulation
Deep Brain Stimulation

Locations

Country Name City State
China Beijing Tian Tan Hospital,Capital Medical University Beijing Beijing
China Tsinghua University Yuquan Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Pins Medical Co., Ltd

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Timed Up and Go (TUG) task variable frequency stimulation (VFS) setting compared to high frequency stimulation (HFS) and low frequency stimulation (LFS) The outcome of TUG task at 12 months follow-up.
Primary the number of freezing episodes for TUG task variable frequency stimulation (VFS) setting compared to high frequency stimulation (HFS) and low frequency stimulation (LFS) The outcome of TUG task at 12 months follow-up.
Secondary UPDRS III scores Outcome of VFS at 6?12 months with reference to baseline HFS
Secondary Gait and Falls Questionnaire (GFQ) scores Outcome of VFS at 6?12 months with reference to baseline HFS
Secondary the39-item Parkinson's Disease Questionnaire (PDQ-39) scores Outcome of VFS at 6?12 months with reference to baseline HFS
Secondary the Freezing of Gait Questionnaire (FOG-Q) scores Outcome of VFS at 6 ?12months with reference to baseline HFS
Secondary Number of adverse events (AE's) Change from Baseline to 6?12 Months
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