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Vacuum-Assisted Clipper in Preoperative Hair Removal: Effects on Contamination and Skin Integrity

StatusNot Yet Recruiting
PhaseNot applicable
Started
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Record History

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  1. Start date: May 1, 2026 to Nov 1, 2026
    • Eligibility criteria expanded, about 17 words
    • Study description revised
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This randomized controlled study aims to evaluate the effectiveness of a vacuum-assisted electric trimmer (VD-ETM) compared with a standard electric trimmer (ETM) for preoperative hair removal. The study will assess microbial and environmental contamination, surgical site infection (SSI), procedure duration, skin integrity, patient safety, and patient satisfaction. Preoperative hair removal is a critical step in preventing SSI; however, conventional ETM devices may contribute to environmental contamination due to dispersed hair particles. VD-ETM systems are designed to reduce this risk by simultaneously removing hair and capturing particles. This study will provide evidence on whether VD-ETM improves operating room hygiene and patient outcomes.
Trial Details
NCT Number NCT07517341
Lead Sponsor Bilecik Seyh Edebali Universitesi
Conditions
(from sponsor)		 Microbial Contamination, Environmental Contamination
Related terms Surgical Wound Infection
Enrollment 120 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov