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MRI Measurement of Lead Location for Suboptimal Outcomes after Deep Brain Stimulation

MRI Measurement of Lead Location for Suboptimal Outcomes after Deep Brain Stimulation - MRI trouble shooting for DBS study (MRI-DBS study)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009996
Enrollment
20
Registered
2013-02-27
Start date
2013-02-04
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson&#39

Interventions

MRI

Sponsors

Juntendo University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Include either 1 or 2: 1. Patients with suboptimal clinical efficacy after DBS therapy. 2. Patients who cannot increase DBS settings due to stimulation induced side effects.

Exclusion criteria

Exclusion criteria: Exclusion criteria are following. 1. Pregnant women and, nursing mothers 2. Patients who have cardiac pacemaker. 3. Patients who cannot understand the concept of this study or who cannot obtain written consent. 4. Patients who are assumed not to be appropriate candidate for this study by investigators.

Design outcomes

Primary

MeasureTime frame
The Parkinson's Disease Questionnaire (PDQ-39)

Secondary

MeasureTime frame
1.Unified Parkinoson's Disease Rating Scale (UPDRS) part I, II, IV 2.UPDRS-III (on/off stimulation, on/off medication) 3. Impedance 4.threshoulds for efficacy and side effect of DBS 5. Beck Depression Inventory (BDI) 6. Hamilton Rating Scale for Depression (HAMD) 7. Montgomery-Asberg Depression Scale (MADRS) 8. Zung Self-rating Depression Scale (SDS) 9. Apathy scale (AS) 10. Mini-Mental State Examination (MMSE) 11. Frontal Assessment Battery (FAB) 12.Japanese version of Montreal Cognitive Assessment (MoCA-J) 13.Keio version Wisconsin card sorting test (KWCST) 14. other complications

Countries

Japan

Contacts

Public ContactGenko Oyama

Juntendo University Department of Neurology

g_oyama@jutendo.ac.jp+81-3-3813-3111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026