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Clinical Trial Summary

The study is designed to investigate the benefit of adding CBME to the existing treatment regime in the management of painful neuropathy. Hypothesis: 1. The addition of CBME to the existing treatment regime will result in a significant improvement in both primary and secondary outcome measures. 2. The side effect profile and tolerability of CBME will be minimal and comparable to placebo.


Clinical Trial Description

1. To investigate the benefit of adding CBME to the existing treatment regime in the management of painful neuropathy. 2. To study the tolerability and side effect profile of CBME. 3. To study the effects of CBME treatment on vibration perception thresholds (VPT) and nerve conduction study parameters. 4. To evaluate the effects of CBME on central nervous system deep nuclei using MR Spectroscopy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00238550
Study type Interventional
Source Sheffield Teaching Hospitals NHS Foundation Trust
Contact
Status Completed
Phase Phase 2
Start date October 2003
Completion date March 2006

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