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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03317509
Other study ID # TMS on Parkinson dysphagia
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 16, 2017
Est. completion date February 20, 2018

Study information

Verified date September 2020
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to assess the therapeutic role of rTMS on parkinson's patients with dysphagia. Thirty PD patients with dysphagia using UK bank criteria for PD will recruited from outpatient clinic in Assuit University. All patients were admitted at Neuropsychiatric Department, Assiut University Hospital/ Assiut, Egypt. Each patient fulfilled the inclusion criteria as spontaneous swallows should be identified clearly when patients cannot perform voluntary swallows using clinical examination test. The patients will be allocated randomly into two groups one of which will receive real sessions of high frequency rTMS (25 HZ), with intensity of 80% of resting motor threshold detected from the hand motor area, with total 2000 pulses for each hemisphere for 10 consecutive sessions totally over period of 10 days with repeated booster session every month during the period of follow up among three months. The other will receive sham sessions. All subjects will be followed up by selected clinical rating scales at different intervals pre session, post 10 sessions, and after one, two and three months.


Description:

This study aims to assess the therapeutic role of repetitive transcranial magnetic (rTMS) on parkinson's patients with dysphagia. Thirty PD patients with dysphagia using UK bank criteria for PD will recruited from outpatient clinic in Assuit University. All patients were admitted at, Neuropsychiatric Department, Assiut University Hospital/ Assiut, Egypt. Each patient fulfilled the inclusion criteria as spontaneous swallows should be identified clearly when patients cannot perform voluntary swallows using clinical examination test. The patients will be allocated randomly into two groups using closed envelops one of which will receive real sessions of high frequency rTMS (25 HZ), with intensity of 80% of resting motor threshold detected from the hand motor area, with total 2000 pulses for each hemisphere for 10 consecutive sessions totally over period of 10 days with repeated booster session every month during the period of follow up among three months. the other will receive sham sessions. All subjects after receiving the rTMS will be followed up by selected clinical rating scales at different intervals Pre session, post 10 sessions, after one, two and three months.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date February 20, 2018
Est. primary completion date February 20, 2018
Accepts healthy volunteers No
Gender All
Age group 50 Years to 75 Years
Eligibility Inclusion Criteria:

- All parkinson's disease patients who were diagnosed according to UK bank criteria for PD, Aged 50-75 years, with dysphagia

Exclusion Criteria:

- History of repeated head injury

- History of repeated cerebrovascular strokes

- History of defined encephalitis

- Oculogyric crisis, supranuclear gaze palsy

- Family history of more than one relative

- History of drug intake as antipsychotics or MPTP exposure

- Severe dementia, (MMSE < 23), Severe depression (H- D) < severe dysautonomia

- Cerebellar signs

- Babiniski sign

- Strictly unilateral features after 3 years

- Hydrocephalus or intracranial lesion on neuroimaging

- We also excluded patients with intracranial metallic devices or with pacemakers or any other device.

- Patients who were unable to give informed Consent because of severe anesthesia or cognitive deficit were not included.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
repetitive transcranial magnetic (rTMS)
Real rTMS high frequency stimulation (25 HZ), with intensity of 80% of resting motor threshold detected from the hand motor area, with total 2000 pulses for each hemisphere for 10 consecutive sessions totally over period of 10 days. Sham rTMS is the same pulse as the first group but with the coil placed perpendicular to the scalp.

Locations

Country Name City State
Egypt Eman Khedr Assiut Assiut, Egypt

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary changes in dysphagia severity measurement Dysphagia severity changes measured by Dysphagia Handicap Index (DHI) Three months
Secondary swallowing changes pre and post 10 sessions using Measurement of swallowing changes pre and post 10 sessions using video fluoroscopy (VFS). ten days