Transvaginal Treatment of Symptomatic Cystocele Grade II-III

Clinical Trial Summary

This observational study will evaluate treatment of symptomatic cystocele grade II-III with Cousin Biomesh and Allium Medical Endofast Reliant. Data about 100 patients will be collected. Follow-up till 3 years after the procedure. Primary endpoint is absence of recurrence.

See also
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NCT number	NCT02272322
Study type	Observational
Source	Regionaal Ziekenhuis Heilig Hart Tienen
Contact
Status	Active, not recruiting
Phase	N/A
Start date	June 2014
Completion date	December 2019

Transvaginal Treatment of Symptomatic Cystocele Grade II-III — BCR

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms