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Clinical Trial Details — Status: Available

Administrative data

NCT number NCT03412539
Other study ID # TASMC-0354-17-TLV
Secondary ID
Status Available
Phase N/A
First received January 21, 2018
Last updated January 21, 2018

Study information

Verified date January 2018
Source Tel-Aviv Sourasky Medical Center
Contact Ido Strauss, MD
Phone 972-3-6974949
Email idos@tlcmc.gov.il
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

The participants in the study are patients who undergo surgery to damaged nerve transmission and processing system in the nervous system as part of the routine clinical treatment that will not be affected by the proposed study. Patients who are candidates for procedures are referred from all over the country and undergo a multidisciplinary evaluation in the framework of the Palliative Pain Management Clinic, which operates exclusively in Israel at the Sourasky Medical Center in Tel Aviv.


Description:

The participants in the study are patients who undergo surgery to damaged nerve transmission and processing system in the nervous system as part of the routine clinical treatment that will not be affected by the proposed study. Patients who are candidates for procedures are referred from all over the country and undergo a multidisciplinary evaluation in the framework of the Palliative Pain Management Clinic, which operates exclusively in Israel at the Sourasky Medical Center in Tel Aviv.

During the preoperative evaluation, patients will be given an explanation about the possibility of participating in the study. Patients who agree to participate will sign an informed consent form.


Recruitment information / eligibility

Status Available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Patients undergoing neurosurgical surgery for resistant pain

- Ability to sign informed consent form for participation in the study

- A functional level is sufficient for cooperation and the performance of various tasks before and after surgery, including performing MRI's, answering pain questioners, and neuropsychological evaluations.

Exclusion Criteria:

- Refusal to participate

- Pregnant women

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Neurosurgery, Tel-Aviv Sourasky MC Tel Aviv

Sponsors (2)

Lead Sponsor Collaborator
Tel-Aviv Sourasky Medical Center University of Haifa

Country where clinical trial is conducted

Israel, 

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