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Trials / Completed

CompletedNCT01109771

Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral Hernia Repair

Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral Hernia Repair (SORBET Trial)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
105 (actual)
Sponsor
University Hospital, Ghent · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To compare the use of absorbable tackers versus permanent tack fixation using a polyester large pore mesh in laparoscopic midline ventral hernia repair in a multicenter (Belgian) prospective randomized single-blinded trial. All patients referred for elective midline ventral hernia repair should be assessed for eligibility and entered in a study log, detailing all included patients during the study period.

Conditions

Interventions

TypeNameDescription
DEVICEpermanent mesh fixationPermanent mesh fixation will be used.
DEVICEabsorbable mesh fixationAbsorbable mesh fixation will be used.

Timeline

Start date
2010-04-01
Primary completion
2015-08-01
Completion
2015-08-31
First posted
2010-04-23
Last updated
2024-07-08

Locations

11 sites across 1 country: Belgium

Source: ClinicalTrials.gov record NCT01109771. Inclusion in this directory is not an endorsement.

Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral Hernia Repair (NCT01109771) · Clinical Trials Directory