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ChloraPrep Versus Betadine for Elective Knee Replacement Surgery

A Comparison of Chlorhexadine Gluconate Versus Povidone Iodine Surgical Preparation in Skin Bacterial Colony Counts for Elective Knee Replacement Surgery

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01184196
Enrollment
55
Registered
2010-08-18
Start date
2009-11-30
Completion date
2012-12-31
Last updated
2013-04-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthroplasty, Knee Replacement, Replacement, Total Knee, Total Knee Replacement

Keywords

knee replacement, knee arthroplasty, total knee replacement, arthroplasty, knee replacement

Brief summary

This study will enroll patients who will be receiving primary total knee replacements. Subjects will be randomized into two groups: Betadine surgical scrub preparation and ChloraPrep preparation prior to total knee replacements. Study hypothesis: When used as a surgical scrub preparation prior to primary total knee arthroplasties, ChloraPrep (2% chlorhexadine gluconate and 70% isopropyl alcohol) is superior to Betadine (10% povidone iodine) in reducing incision site bacterial colony counts.

Detailed description

Swabs will be taken over the operative knee by study personnel for a bacterial colony count immediately before surgical site preparation is started, after the surgery prep is complete, and 24 hours post surgery prep. Swabs will be sent to the lab for quantitative colony counts and all 3 measurements will be compared and analyzed.

Interventions

DRUGSwab area with Betadine

A swab will be taken over the operative knee before surgical site preparation is started, after preparation has taken place, and 24 hours post-surgery.

DRUGSwab area with ChloraPrep

A swab will be taken over the operative knee before surgical site preparation is started, after preparation has taken place, and 24 hours post-surgery.

Sponsors

Central DuPage Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Scheduled to undergo primary total knee arthroplasty * Age 18 or over

Exclusion criteria

* Inability to provide informed consent or to comply with study assessments due to cognitive impairment or geographic distance * Age 17 or younger * Allergies to chlorhexadine gluconate or povidone iodine * Topical antimicrobial use within 14 days of surgery * Any active dermatoses or open wounds over the operative site * Any condition requiring antibiotics 14 days prior to arriving for surgery * Patients with chronic immunosuppression (such as HIV/AIDS) * Unable to adhere to follow up schedule and treatment

Design outcomes

Primary

MeasureTime frameDescription
Quantitative bacterial colony counts for aerobic and anaerobic culture swabs will be taken at 3 timeperiods to determine if ChloraPrep is superior to Betadine in reducing incision site bacterial colony counts.24 hoursSubjects scheduled to undergo primary total knee arthroplasty will be randomized to receive either a Betadine surgical scrub or ChloraPrep surgical scrub at the time of surgery. Subjects will be enrolled until swab #3 is obtained, 24 hours post-surgery.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026