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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03263884 |
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Date of registration:
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24/08/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Repetitive Transcranial Magnetic Stimulation and the Development of Ongoing Muscle Pain
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Scientific title:
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Repetitive Transcranial Magnetic Stimulation and the Development of Ongoing Muscle Pain |
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Date of first enrolment:
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August 1, 2017 |
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Target sample size:
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30 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03263884 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Single (Participant).
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Phase:
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N/A
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Countries of recruitment
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Denmark
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Contacts
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Name:
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Enrico De Martino, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Aalborg University |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Healthy men and women
- Speak and understand English.
Exclusion Criteria:
- Pregnancy
- Drug addiction defined as the use of cannabis, opioids or other drugs
- Previous neurologic, musculoskeletal or mental illnesses
- Lack of ability to cooperate
- History of chronic pain or current acute pain
- Previous experience with rTMS
- Contraindications to rTMS application (history of epilepsy, metal in the head or jaw
etc.).
- Failure to pass the "TASS questionnaire" (TASS = Transcranial Magnetic Stimulation
Adult Safety Screen)
Age minimum:
21 Years
Age maximum:
50 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Pain Relief
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Intervention(s)
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Device: Repetitive trancranial magnetic stimulation (rTMS) group
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Device: Sham group
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Primary Outcome(s)
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Pain relief
[Time Frame: Change from baseline at 2 weeks]
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Secondary Outcome(s)
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Cuff pressure algometry
[Time Frame: Change from baseline at 2 weeks]
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Attention network test
[Time Frame: Change from baseline at 2 weeks]
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Muscle soreness
[Time Frame: Change from baseline at 2 weeks]
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EEG recordings
[Time Frame: Change from baseline at 1 weeks]
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Pressure pain thresholds
[Time Frame: Change from baseline at 2 weeks]
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Patient-rated Tennis Elbow Evaluation
[Time Frame: Change from baseline at 2 weeks]
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Secondary ID(s)
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N-20170041
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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