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Clinical Trial Summary

Patients arriving to rehabilitation up to 2 months following SCI will be given (study group) or not (control group) Lyrica (75X2). They will be followed for central pain development.


Clinical Trial Description

Patients arriving to rehabilitation up to 2 months following SCI will be recruited, if they have not yet developed central pain. Two thirds (the study group) will be treated with Lyrica (Pregabalin75X2) for 3 months. One third (the control group) will not receive preventative treatment. Participants will be followed for central pain development. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06066918
Study type Interventional
Source Loewenstein Hospital
Contact Amiram Catz, Dr
Phone 972-9-770-9934
Email amiramc@clalit.org.il
Status Recruiting
Phase N/A
Start date July 13, 2021
Completion date February 5, 2026

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