Deep rTMS in Parkinson Disease Pain Syndromes
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| ClinicalTrials.gov Identifier: NCT03504748 |
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Recruitment Status : Unknown
Verified May 2018 by Daniel Ciampi Araujo de Andrade, MD, PhD, University of Sao Paulo.
Recruitment status was: Recruiting
First Posted : April 20, 2018
Last Update Posted : May 8, 2018
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Pain Parkinson Disease | Device: deep rTMS Device: placebo deep rTMS | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 30 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Double (Participant, Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | Deep rTMS in Parkinson Disease Pain Syndromes |
| Actual Study Start Date : | July 20, 2015 |
| Estimated Primary Completion Date : | July 2018 |
| Estimated Study Completion Date : | December 2018 |
| Arm | Intervention/treatment |
|---|---|
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Active Comparator: deep rTMS-active doble coil
patients undergoing of deep rTMS real with doble coil
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Device: deep rTMS |
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Sham Comparator: deep rTMS-sham
patients undergoing to placebo deep rTMS
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Device: placebo deep rTMS |
- Change in baseline of Pain [ Time Frame: base line (moment of inclusion), day 15th, day 45th and in the last day of the sessions of rTMS (4X in two months) ]assessing by Visual Analog Scale for Pain (VAS). This scale range from 0 (no pain) to 10 (maximum pain), being considered an effective improvement in the patient's pain when the pain decreases at least in 30% from the basal score.
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| Ages Eligible for Study: | 18 Years to 80 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Parkinson disease
- Signed term of informed consent
- Parkinsson disease related pain
Exclusion Criteria:
- Trauma of Skull, epilepsy don't treated
- Use of medications decrease the seizure threshold
- Patients in use of drugs, how cocaine and alcohol
- neurosurgical clips, pacemakers, increased intracranial pressure (risk of sequelae after seizure)
- Pregnant or lacting women
- Moderate or severe cognitive impairment
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03504748
| Contact: Daniel MD Ciampi, Phd | + 55 11 997753538 | ciampi@usp.br | |
| Contact: Victor MD Barboza, PhD student | + 55 11 997017706 | victors.rb@gmail.com |
| Brazil | |
| Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HC/FMUSP) | Recruiting |
| São Paulo, SP, Brazil, 05403900 | |
| Contact: Daniel MD Ciampi, Phd + 55 11 997753538 ciampi@usp.br | |
| Responsible Party: | Daniel Ciampi Araujo de Andrade, MD, PhD, MD, PhD (Head of Pain Division), University of Sao Paulo |
| ClinicalTrials.gov Identifier: | NCT03504748 |
| Other Study ID Numbers: |
VRBDCA |
| First Posted: | April 20, 2018 Key Record Dates |
| Last Update Posted: | May 8, 2018 |
| Last Verified: | May 2018 |
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deep repetitive transcranial magnetic stimulation chronic pain parkinson treatment non-motor symptom |
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Parkinson Disease Parkinsonian Disorders Basal Ganglia Diseases Brain Diseases Central Nervous System Diseases |
Nervous System Diseases Movement Disorders Synucleinopathies Neurodegenerative Diseases |

