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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00416247
Other study ID # rambam2409_CTIL
Secondary ID
Status Completed
Phase N/A
First received December 26, 2006
Last updated August 4, 2010
Start date December 2006
Est. completion date June 2009

Study information

Verified date December 2006
Source Rambam Health Care Campus
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

This study is intended to investigate neurophysiological mechanisms of hypnosis using transcranial magnetic stimulation (TMS) and assessment of motor cortex excitability in healthy volunteers under hypnosis.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 2009
Est. primary completion date December 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria: .

1. Healthy volunteers aged 20 to 45 years.

2. Hypnotisability above 14 as measured by the Tellegan absorption scale.

Exclusion Criteria:

1. Psychiatric diagnosis in axis I or axis II;

2. Documented history of head injury or seizure disorder;

3. Evidence of a disorder which could affect peripheral and central conduction such as multiple sclerosis, motor neuron disease, carpal tunnel syndrome, cervical spondylosis, diabetic neuropathy.

4. Any other contraindication to TMS as specified in the safety guidelines for rTMS (Wassermann, 1998) such as cardiac pacemakers or metallic deep brain electrodes.

5. Chronic pharmacological treatment.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Behavioral:
Hypnosis
Hypnosis

Locations

Country Name City State
Israel Rambam Medical Center Haifa

Sponsors (1)

Lead Sponsor Collaborator
Rambam Health Care Campus

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cortical Excitability Before and after intervention No
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