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Pre-surgical Antisepsis Using an Alcoholic Solution of Chlorhexidine Digluconate and Potassium Sorbate ( Sorbectol )

NCT04683146 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2020-12-24

No results posted yet for this study

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.

Conditions

  • Antisepsis

Interventions

DRUG

Hand antisepsis with Propanolol- 1 60%.

* Pre-washing for one minute with neutral soap to remove the transient flora. * Hand antisepsis using Propanolol-1 60% in both hands. * Bacterial sample collection from right hand. * Sterile surgical glove in both hands. * Bacterial sample collection from left hand three hours later

DRUG

Hand antisepsis with a solution of alcohol, chlorhexidine digluconate and potassium sorbate.

* Pre-washing for one minute with neutral soap to remove the transient flora. * Hand antisepsis using a solution of alcohol, chlorhexidine digluconate and potassium sorbate. * Bacterial sample collection from right hand. * Sterile surgical glove in both hands. * Bacterial sample collection from left hand three hours later.

Sponsors & Collaborators

  • Centro Ortopedico y Quirurgico del Pie

    lead OTHER

Principal Investigators

  • Ricardo Becerro de Bengoa Vallejo · Universidad Complutense de Madrid

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-03-10
Primary Completion
2021-03-24
Completion
2021-06-05

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04683146 on ClinicalTrials.gov