送交者: 猎人 于 2011-04-10, 19:38:55:
Official Title: Lumbar to Sacral Ventral Nerve Re-Routing
Study Design: Endpoint Classification: Efficacy Study
Primary Outcome Measures: Assess the level of improvement in voiding function after lumbar to sacral ventral nerve re-routing procedure in SCI and spina bifida patients. [time frame: evaluated at 6 months and 1 year ][designated as safety issue: no]
第二个试验(NCT01096459)：
Official Title: Safety and Efficacy of Nerve Rerouting for Treating Neurogenic Bladder in Spina Bifida
Study Design: Endpoint Classification: Safety/Efficacy Study
Primary Outcome Measures: Reproducible bladder contraction [time frame: 6 to 24 months post procedure] [designated as safety issue: yes]
Secondary Outcome Measures: Transfer of knowledge to other personnel to learn the procedure [time frame: two years] [designated as safety issue: yes].