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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04454619
Other study ID # RICBEC
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date July 12, 2020
Est. completion date August 15, 2020

Study information

Verified date August 2020
Source Centro Ortopedico y Quirurgico del Pie
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The present study evaluates the effects of bactericidal load reduction after surgical hand scrub antisepsis using the reference antiseptic product propan-ol-1 60% as control versus a surgical hand scrub antisepsis with addition of a solution of chlorhexidine digluconate and potassium sorbate in order to test if pass the standard european norm 12791.


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 addition of a solution of 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.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date August 15, 2020
Est. primary completion date July 18, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Participants without systemic pathologies, with healthy skin of the hands and short fingernails.

- They do not use substances with antibacterial action.

Exclusion Criteria:

- Taken antibiotics before 10 days of the intervention.

- Wear any jewellery on the hands

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Hand antisepsis with Clorhexidine and solution
Hand antisepsis by scrub Surgical Hand scrubbing using chlorhexidine digluconate with the addition of an alcoholic solution of chlorhexidine digluconate and potassium sorbate. both hands using a sterile disposable surgical scrub brush with plastic bristles on one side and a foam sponge on the other side

Locations

Country Name City State
Spain Centro ortopedico y quirurgico del pie Madrid Madrid.

Sponsors (1)

Lead Sponsor Collaborator
Centro Ortopedico y Quirurgico del Pie

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of bacterial load measured in CFU immediately after hand scrub Participants will scrub the antiseptic solution vigorously from hand to the wrists according with the standard handrub procedure Change from bacterial load at 5 minutes
Secondary Change of bacterial loadmeaured in CFU after 3 hours of hand scrub Participants will scrub the antiseptic solution vigorously from hand to the wrists according with the standard handrub procedure after 3 hours Change from bacterial load at 3 hours
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
Not yet recruiting NCT04683146 - Pre-surgical Antisepsis Using an Alcoholic Solution of Chlorhexidine Digluconate and Potassium Sorbate ( Sorbectol ) Phase 4
Completed NCT05896462 - Effect of Skin Antisepsis After Skin Closure on Wound Infection After Abdominal Surgery for Sepsis: a Preliminary Report N/A