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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: |
NCT03074422 |
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Date of registration:
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03/03/2017 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Effectiveness and Reliability of Hypnosis in Stereotaxy
ERST |
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Scientific title:
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Effectiveness and Reliability of Hypnosis in Stereotaxy |
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Date of first enrolment:
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July 1, 2017 |
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Target sample size:
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22 |
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Recruitment status: |
Unknown status |
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URL:
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https://clinicaltrials.gov/show/NCT03074422 |
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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: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Switzerland
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Contacts
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Name:
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Marco Corniola |
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Address:
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Telephone:
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Email:
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Affiliation:
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University Hospital, Geneva |
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Name:
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Marco Corniola |
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Address:
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Telephone:
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795533770 |
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Email:
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marco.corniola@hcuge.ch |
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Affiliation:
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Name:
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Marco Corniola |
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Address:
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Telephone:
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0795533770 |
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Email:
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marco.corniola@hcuge.ch |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients undergoing a stereotactic procedure as listed previously
- Patients = 18 y.o.
Exclusion Criteria:
- Patients < 18 y.o.
- Patients unable to take decisions by their own
- Patients undergoing deep brain stimulation for obsessive-compulsive disease treatment
- Patients refusing to participate to the study
- Pregnancy
- Invasive monitoring of epilepsy
- Psychiatric comorbidity
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Dystonia, Primary
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Tremor, Essential
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Parkinson Disease
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Intervention(s)
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Procedure: Hypnosis
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Primary Outcome(s)
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Effect on pain
[Time Frame: 2 years]
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Secondary Outcome(s)
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Effect on the stress perceived during the procedure
[Time Frame: 2 years]
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Effect on the incidence of post-traumatic stress disorder
[Time Frame: 2 years]
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Secondary ID(s)
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2016-01843
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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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