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Clinical Trial Summary

This prospective study evaluates celiac plexus radiosurgery for pain control in patients with upper abdominal malignancies.


Clinical Trial Description

This study aims as primary objective to evaluate short and long term pain relief following the administration of radiosurgery to the celiac plexus in patients with upper abdominal cancer. As secondary objectives it will describe acute and late side effects and quality of life measures of patients undergoing the treatment.

The study has a prospective, single arm design. It will be composed from an initial run-in safety assessment that will include 6 patients and then continue as a phase II trial. All eligible patients will receive the same protocol of celiac plexus radiosurgery and will be evaluated before, during and following this treatment.

The treatment duration is one and a half weeks (5 fractions delivered every other weekday). ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT02356406
Study type Interventional
Source Sheba Medical Center
Contact David Hausner, M.D
Phone 972-35302542
Email david.hausner@sheba.health.gov.il
Status Recruiting
Phase Phase 2
Start date January 2014
Completion date June 2016

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