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Antiseptic

Chlorhexidine gluconate bathing for Surgical Site Infection

N/A
Waitlist Available
Led By Joshua T Swan, Pharm.D.
Research Sponsored by Joshua Swan
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 28 days
Awards & highlights
Approved for 5 Other Conditions
All Individual Drugs Already Approved

Summary

This prospective, randomized, controlled trial will compare the incidence of nosocomial infections (composite of primary bloodstream infections, catheter-associated urinary tract infections, ventilator-associated pneumonia, and surgical site infections) that occur in intensive care unit (ICU) patients bathed with 2% chlorhexidine solution versus patients who receive standard bathing (soap and water or non-medicated cloths).

Eligible Conditions
  • Ventilator-associated pneumonia
  • Surgical Site Infection
  • Catheter-associated urinary tract infection
  • Community-Acquired Infections
  • Cross Contamination

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 28 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 28 days for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Incidence of Nosocomial Infection
Secondary study objectives
ICU Length of Stay in Days
Incidence of Skin Irritation

Awards & Highlights

Approved for 5 Other Conditions
This treatment demonstrated efficacy for 5 other conditions.
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Chlorhexidine gluconate bathingActive Control1 Intervention
Upon study enrollment, patients will be bathed with a 2% chlorhexidine gluconate solution on study day 1 and every 48 hours until study completion. The patient will be bathed using standard bathing (non-medicated cloths or soap and water) on study day 2 and every 48 hours after that.
Group II: Standard bathingPlacebo Group1 Intervention
Upon study enrollment, patients will be bathed using standard bathing (non-medicated cloths or soap and water) daily.

Find a Location

Who is running the clinical trial?

Texas Southern UniversityOTHER
Joshua SwanLead Sponsor
The Methodist Hospital Research InstituteOTHER
286 Previous Clinical Trials
81,398 Total Patients Enrolled
~26 spots leftby Nov 2025