Intra-operative Adverse Events During Laparoscopic Ventral Mesh Rectopexy

Status Not yet recruiting

Clinical Trial Summary

Outcomes of laparoscopic ventral mesh rectopexy are well known, but data on intra-operative adverse events is scant. A multicenter pool-analysis of prospectively collected database on 1384 patients with internal/external rectal prolapse toke place. Overall 72 (5%) patients experienced complications, 41 discovered and managed intraoperatively, 22 postoperative complications, and 9 required readmission. Despite accepted lower rate of morbidity, these results come from four well equipped European centers by four surgeons practiced at least 200 LVMR.

Clinical Trial Description

Multicenter pooled-analysis of LVMR for internal/external rectal prolapse. All events occurred and discovered intra-operatively or passed undiagnosed and appeared within 30-days postoperatively (same admission/readmission) will included, with classification according to the Clavien-Dindo classification. ;

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02870192
Study type	Interventional
Source	University of Rome Tor Vergata
Contact	Mostafa Shalaby, MD, MSc
Phone	0039329353441
Email	shalaby-mostafa@hotmail.com
Status	Not yet recruiting
Phase	N/A
Start date	January 2017
Completion date	January 2018

View Details

See also
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