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Clinical Trials in Turkey / NCT06801275
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The Effect of Number of Showers With 4% Chlorhexidine Gluconate on Prevention of Surgical Site Infections

NCT06801275 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-07-01
Last updated
2025-09-17

Condition(s) studied

Surgical Site InfectionsLumbar Disc Herniation

Investigational drug(s) / intervention(s)

1 shower with 4% chlorhexidine gluconate2 shower with 4% chlorhexidine gluconate

1 shower with 4% chlorhexidine gluconate: Comparison of the effect of showering once with 4% Chlorhexidine Gluconate before lumbar disc herniation surgery on surgical site infections

2 shower with 4% chlorhexidine gluconate: Comparison of the effect of showering twice with 4% Chlorhexidine Gluconate before lumbar disc herniation surgery on surgical site infections

Study summary

Surgical site infections (SSIs) are the most common type of nosocomial infection in surgical departments.

Although lumbar disc herniation (LDH), which is one of the common cases in neurosurgery, is a serious problem affecting postoperative SSI, morbidity and mortality, there are not enough studies on its prevention in the literature.

In the literature, there are studies on showering with chlorhexidine or other antiseptic solutions in the preoperative period to prevent SSI, but there is no study on whether the number of showers performed in the preoperative period is effective on SSI.

In this study, the effect of showering with 4% chlorhexidine gluconate before lumbar disc herniation surgery on postoperative surgical site infections will be examined. It is aimed to compare the effect of douching with 4% Chlorhexidine Gluconate before lumbar disc hernia surgery on surgical site infections. Since there are not enough studies in the literature, this study is an innovative study. In this study, it is thought that washing the surgical site with antiseptic soap containing 4% Chlorhexidine Gluconate before LDH surgery will have an effect on surgical site infections.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * to communicate verbally Exclusion Criteria: * Patients with diabetes mellitus side disease, pylolidal cyst surgery, any surgical history from the lumbar region and patients who will undergo lumbar disc hernia stabilisation surgery will not be included.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Çanakkale on Sekiz Mart University Çanakkale Merkez
Çanakkale on Sekiz Mart Üniversity Çanakkale Merkez

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06801275 on ClinicalTrials.gov ↗ ← All trials in Turkey