Clinical Trials Directory

Trials / Terminated

TerminatedNCT02083939

Prophylactic Antibiotic Treatment for Laparoscopic Inguinal Hernia Mesh Repair: Necessary or Not?

Status
Terminated
Phase
Study type
Observational
Enrollment
5 (actual)
Sponsor
Sheba Medical Center · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to find out whether it is necessary to prophylactically treat patients undergoing laparoscopic inguinal hernia repairs with antibiotics. Our hypothesis is that it is not necessary to pretreat patients with antibiotics if the operation is minimally invasive with a mesh placed at the defect.

Detailed description

The investigators plan to follow up at least 100 patients who did not receive antibiotics prior to their inguinal hernia repair and compare their outcome to 100 patients who did receive prophylaxis. The investigators mainly will be analyzing the incidence of surgical site infections as evidenced by swelling, redness, pain, warmth or other signs deemed by the surgeon.

Conditions

Timeline

Start date
2014-03-01
Primary completion
2019-09-17
Completion
2019-09-17
First posted
2014-03-11
Last updated
2020-06-04

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT02083939. Inclusion in this directory is not an endorsement.

Prophylactic Antibiotic Treatment for Laparoscopic Inguinal Hernia Mesh Repair: Necessary or Not? (NCT02083939) · Clinical Trials Directory