Study of Autologous Neo-Bladder Construct in Subjects With Neurogenic Bladder Following Spinal Cord Injury
Stopped early · Phase 2
Conditions studied: Neurogenic Bladder
In brief
Subjects with neurogenic bladder secondary to spinal cord injury that is refractory to medical treatment and requires augmentation cystoplasty will be enrolled. The hypothesis is that augmentation cystoplasty using an autologous neo-bladder construct will reduce maximum detrusor pressure.
Key facts
- Study ID
- NCT00512148
- Run by
- Tengion
- People needed
- 7
- Starts
- 2007-07-01
- Expected to finish
- 2011-04-01
- Last updated by the study team
- 2018-08-17
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- subjects with neurogenic bladders secondary to spinal cord injury
You may not qualify if…
- prior augmentation procedures or urinary diversion
- recent urologic or intraperitoneal surgery or device implantation
- recent history of spinal cord injury of less than a year
- recent neurologic surgery
- requirement for concomitant urological surgical procedures
Where it is running
- Thomas Jefferson University Hospital — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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