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Clinical Trial Summary

The present study evaluates the effects of bactericidal load reduction after surgical hand antisepsis using the reference antiseptic product propanol- 1 60% as control versus a surgical hand antisepsis with addition of a solution of alcohol, chlorhexidine digluconate and potassium sorbate 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 surgical hand antisepsis using propan-ol-1 60% by using the reference antiseptic product propan-ol-1 60% as control versus a surgical hand antisepsis with addition of a solution of alcohol, chlorhexidine digluconate and potassium sorbate 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 NCT04683146
Study type Interventional
Source Centro Ortopedico y Quirurgico del Pie
Contact Ricardo Becerro de Bengoa Vallejo
Phone +34 670678145
Email ribebeva@ucm.es
Status Not yet recruiting
Phase Phase 4
Start date March 10, 2021
Completion date June 5, 2021

See also
  Status Clinical Trial Phase
Completed NCT04538365 - Pre-surgical Antisepsis of Hands After Washing With Triclosan 0.5% Compared to Propan-1-ol 60% Phase 4
Completed NCT02833376 - Alcohol 70% Versus Chlorhexidine 0.5% in the Spinal Anesthesia Skin Antissepsis N/A
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