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Clinical Trial Summary

The present study evaluates the effects of bactericidal load reduction after surgical hand scrub antisepsis using the reference antiseptic product propanol- 1 60% as control versus a surgical hand scrub antisepsis with triclosan 0.5% in order to test if pass the standard european norm 12791.


Clinical Trial Description

The investigators conducted a crossover clinical trial to evaluate the antiseptic effectiveness of preoperative surgical scrubbing using propan-ol-1 60% by scrub using the reference antiseptic product propan-ol-1 60% as control versus a surgical hand scrub antisepsis with trocilosan 0.5% in order to test if pass the standard european norm 12791. Samples will be taken from the hands of each volunteer after a surgical hands antiseptic. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04538365
Study type Interventional
Source Centro Ortopedico y Quirurgico del Pie
Contact
Status Completed
Phase Phase 4
Start date October 1, 2020
Completion date October 30, 2020

See also
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Not yet recruiting NCT04683146 - Pre-surgical Antisepsis Using an Alcoholic Solution of Chlorhexidine Digluconate and Potassium Sorbate ( Sorbectol ) Phase 4
Completed NCT04454619 - Pre-surgical Antisepsis Using an Alcoholic Solution of Chlorhexidine Digluconate and Potassium Sorbate Phase 4
Completed NCT05896462 - Effect of Skin Antisepsis After Skin Closure on Wound Infection After Abdominal Surgery for Sepsis: a Preliminary Report N/A