Clinical Trials Directory

Trials / Completed

CompletedNCT07111702

Prophylactic Antibiotics in Groin Hernioplasty

Prophylactic Antibiotics in Groin Hernioplasty: A Prospective Cohort Study on the Prevention of Surgical Site Infection

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Sana'a University · Academic / Other
Sex
Male
Age
17 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The role of prophylactic antibiotics in preventing surgical site infections (SSI) for clean procedures like groin hernia repair remains controversial. This study aimed to evaluate the association between antibiotic prophylaxis and SSI rates in a real-world clinical setting and to identify independent risk factors for SSI. The study prospectively followed 100 male patients undergoing elective open groin hernioplasty. Patients were categorized based on the surgeon's decision into two groups: those who received a single dose of intravenous cefazolin (Antibiotic Group) and those who did not (No Antibiotic Group). The main outcome was the rate of SSI within 30 days of surgery.

Conditions

Interventions

TypeNameDescription
DRUGCefazolinA single 2g intravenous dose administered once before surgery.

Timeline

Start date
2023-10-01
Primary completion
2024-05-30
Completion
2024-05-30
First posted
2025-08-08
Last updated
2025-08-13

Locations

1 site across 1 country: Yemen

Source: ClinicalTrials.gov record NCT07111702. Inclusion in this directory is not an endorsement.