Clinical Trials Directory

Trials / Completed

CompletedNCT01195545

Veritas Laparoscopic Paraesophageal Hiatal Hernia (PEH) Repair Pilot Trial

Veritas Laparoscopic PEH Repair Pilot Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
University of Washington · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is an investigator initiated pilot study to observe the short-term outcomes (a follow-up period of up to six months) of patients who undergo a laparoscopic paraesophageal Hiatal hernia (PEH) repair using the Veritas® Collagen Matrix brand biological mesh. This is a preliminary study at the University of Washington. A PEH occurs when the stomach protrudes through the diaphragm next to the esophagus. The chance of recurrence of a Hiatal hernia after laparoscopic PEH repair is between 20-40% within 6 months.During laparoscopic PEH repair, a mesh-type product is used as a scaffold. The mesh serves as a reinforcing material during the surgical repair. It is cut to the appropriate size needed for the hernia and sutured to the surrounding diaphragmatic tissue. There are many different types of meshes available on the market, and vary in the degree of manageability, strength, and adherence. Although surgical meshes work on the same principal, the variance between materials may affect patient outcomes. There is evidence that a biologic mesh, specifically one derived from Small Intestinal Submucosa (SIS), decreases the short-term (6-month) recurrence rates compared to a synthetic mesh or another type of biologic mesh. A biologic mesh, serving as a scaffold, will be replaced by the patient's own tissue after about 6 months. Theoretically, this would prevent the possible complications associated with synthetic mesh including mesh erosion into the esophagus or stricture of the esophagus. There are some case series showing similar short-term results between the different biologic meshes, but there is no direct comparative data.

Conditions

Interventions

TypeNameDescription
DEVICEVeritas® Collagen Matrixbiological mesh in hernia repair

Timeline

Start date
2010-05-01
Primary completion
2012-12-01
Completion
2013-12-01
First posted
2010-09-06
Last updated
2018-07-10
Results posted
2018-07-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01195545. Inclusion in this directory is not an endorsement.