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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05401292
Other study ID # 2074962
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date February 15, 2022
Est. completion date December 2025

Study information

Verified date July 2023
Source University of Missouri-Columbia
Contact Stacee Baker, MEd, BSN, RN
Phone 5738849017
Email staceebaker@health.missouri.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Surgical site infections (SSIs) make about 31% of all nosocomial infections and they are the most common hospital-acquired infection. For foot and ankle elective interventions, SSI rate is reported between 0.4% and 3.6%. This study will investigate the effectiveness of skin cleaning with isopropyl alcohol and scrubbing with chlorhexidine soap before standard skin preparation in reducing microbial load and surgical site infections for elective foot and ankle surgeries. Current standard of care includes skin preparation with iodine or chlorhexidine solution prior to sterile draping and the start of surgery. Standard of care will be applied to all patients. The use of an additional "pre-scrub" with isopropyl alcohol and scrubbing with chlorhexidine soap will be applied to the experimental group. The control group will receive only the standard of care skin preparation with iodine or chlorhexidine solution prior to draping.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2025
Est. primary completion date December 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients undergoing elective foot and ankle surgeries - age over 18 Exclusion Criteria: - trauma as the indication for surgery - open injuries - non-elective procedures - amputations - prior surgical site infection through the planned incision - pregnancy. All potential participants of child-bearing potential follow the standard pre-operative protocol to ensure they are not in pregnant status prior to SOC surgical procedure.

Study Design


Intervention

Drug:
Hibiclens
antiseptic/antimicrobial skin cleanser for skin wound and general skin cleansing
Isopropyl Alcohol 70% Topical Application Solution
First aid antiseptic

Locations

Country Name City State
United States University of Missouri Columbia Missouri

Sponsors (1)

Lead Sponsor Collaborator
University of Missouri-Columbia

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Surgical Site Infection rate of surgical site infection (SSI) and wound complications following skin preparation for surgery. Measured by the number of surgical site infections in the total population of patients in the cohort 90 days
Secondary Microbial Load effectiveness of reducing microbial load. Comparing original microbial load to final microbial load (CFU/g) 90 days
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