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Prevention of Catheter-Associated Infection With the Skin Disinfectant Octenidine Dihydrochloride

Primary Purpose

Catheterization, Central Venous, Catheter-Associated Infections, Bacterial Infections

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
0.1% Octenidine with 30% 1-propanol and 45% 2-propanol
74% Ethanol with 10% 2-propanol
Sponsored by
University Hospital Freiburg
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Catheterization, Central Venous focused on measuring Bloodstream Infection, Bacteremia, Central Venous Catheter, Alcohol, Disinfection, Octenidine Dihydrochloride

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients >18 years
  • Medical indication for CVC with a planned duration of minimum 5 days
  • Patient´s (or relative´s if applicable) written informed consent

Exclusion Criteria:

  • Known sensitisation against the proposed antiseptics
  • Tunneled or implanted CVCs (e.g. Hickman Catheter)
  • Administration of antimicrobial drugs for therapy (not prophylaxis) less than one week prior to catheterization
  • Pre-existing bloodstream infection (i.e., fever and/or other signs of infection)
  • Positive blood culture
  • Terminal patients with limited therapy options
  • Patients with burns
  • Patients participating in a clinical trial on other antiseptics within a period of four weeks prior to inclusion date
  • Patients with missing written consent

Sites / Locations

  • Institute of Environmental Medicine and Hospital Epidemiology University Medical Center Freiburg
  • Division of Infectious Diseases and Hospital Epidemiology, University Hospital Basel

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Oct/Alc

Alc

Arm Description

Outcomes

Primary Outcome Measures

Skin colonisation in cfu/cm2 at the insertion site; Colonisation of the CVC-tip, positivity by definition of number cfu/5cm > 15 (Maki-method); Incidence of catheter-associated bloodstream infection

Secondary Outcome Measures

Comparison of therapy regimens regarding side effects and complications

Full Information

First Posted
August 10, 2007
Last Updated
August 10, 2007
Sponsor
University Hospital Freiburg
Collaborators
University Hospital, Basel, Switzerland
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1. Study Identification

Unique Protocol Identification Number
NCT00515151
Brief Title
Prevention of Catheter-Associated Infection With the Skin Disinfectant Octenidine Dihydrochloride
Official Title
Skin Disinfection With Octenidine Dihydrochloride for the Prevention of Catheter-Associated Infections - A Double-Blind, Randomized, Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2007
Overall Recruitment Status
Completed
Study Start Date
May 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2005 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University Hospital Freiburg
Collaborators
University Hospital, Basel, Switzerland

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Health-care-acquired infections are of tremendous importance for patients, especially catheter-associated infections. More than 40% of all bloodstream infections are associated with central venous catheters (CVC; catheters which are inserted into a large vein near the heart). Of all patients that acquire such an infection 1% to 5% die as a result from it. The insertion site is the main source of contamination and infection. In general, bacteria of the skin are the cause of infection, especially in short-term CVCs (10-14 days). Therefore it is necessary to efficiently disinfect the skin for the preparation and care of CVC insertion sites. Several substances are used for disinfection. Alcohol-based disinfectants are mainly used in Central Europe, other preparations contain povidine-iodine or chlorhexidine. Alcoholic disinfectants have a rapid initial effect, chlorhexidine shows an additional remanent (longer lasting) effect. A further substance, octenidine dihydrochloride, also demonstrated a remanent effect in a pilot study with neurosurgical patients. The purpose of our study is to compare an alcohol-based disinfectant containing octenidine dihydrochloride with a pure alcoholic disinfectant regarding efficacy and tolerability in patients receiving a CVC for a minimum of 5 days.
Detailed Description
Catheter-associated infections are one of the most eminent healthcare acquired infections. More than 40% of all bloodstream infections are associated with a central venous catheter (CVC)and between 1% and 5% of the affected patients die as a direct consequence of this infection. The most important microorganisms are gram-positive cocci (S. aureus, S. epidermidis). In intensive care units gram-negative microorganisms such as pseudomonas, acinetobacter and candida spp. are more frequent. The insertion site is the main source of contamination and infection in short-term CVCs (10-14 days. In this case the infection is caused by migration of microorganisms along the outside of the catheter. Contamination of the hub due to frequent manipulation is usually the source of infection in long-term CVCs. In this case the infection occurs intraluminally. An effective skin disinfection is the main measure of prevention before insertion of a CVC. The aim of this measure is the elimination of transient and the reduction of resident microorganisms around the insertion site. To achieve this, disinfectants on the basis of alcohol, povidone-iodine or chlorhexidine are applied. Alcohol-based disinfectants are preferred in Central Europe because of their rapid initial effect and broad microbiological spectrum. Chlorhexidine and povidone-Iodine in contrast to alcoholic disinfectants have a remanent effect which reduces regrowth of microorganisms beyond the immediate initial effect. To which extent remanent substances reduce colonization of the CVC extraluminally or the CVC-tip is still being disputed. In an earlier clinical trial a residual or remanent effect of 0.1% octenidine combined with propanol in microbial skin decontamination over a 24h period was shown in neurosurgical patients receiving a central line (CVC or peripherally inserted central catheter). The objective of this study is therefore to evaluate further the preventive impact and tolerability of a commercially available, alcohol-based antiseptic solution containing octenidine for the preparation and care of CVC insertion sites in a clinical setting in comparison with the results given by an alcoholic solution alone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Catheterization, Central Venous, Catheter-Associated Infections, Bacterial Infections, Bacteremia
Keywords
Bloodstream Infection, Bacteremia, Central Venous Catheter, Alcohol, Disinfection, Octenidine Dihydrochloride

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
400 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Oct/Alc
Arm Type
Active Comparator
Arm Title
Alc
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
0.1% Octenidine with 30% 1-propanol and 45% 2-propanol
Other Intervention Name(s)
Octeniderm, Neo-Kodan
Intervention Description
Before insertion of the catheter, the entry site was disinfected with the assigned solution over an area of >200 cm² for at least one minute. The assigned solution was then applied for care of the entry site during the change of dressings, usually every 2 to 3 days.
Intervention Type
Drug
Intervention Name(s)
74% Ethanol with 10% 2-propanol
Other Intervention Name(s)
Softasept
Intervention Description
Before insertion of the catheter, the entry site was disinfected with the assigned solution over an area of >200 cm² for at least one minute. The assigned solution was then applied for care of the entry site during the change of dressings, usually every 2 to 3 days.
Primary Outcome Measure Information:
Title
Skin colonisation in cfu/cm2 at the insertion site; Colonisation of the CVC-tip, positivity by definition of number cfu/5cm > 15 (Maki-method); Incidence of catheter-associated bloodstream infection
Time Frame
For the duration of catheter placement plus 2 days
Secondary Outcome Measure Information:
Title
Comparison of therapy regimens regarding side effects and complications
Time Frame
For the duration of catheter placement plus 30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients >18 years Medical indication for CVC with a planned duration of minimum 5 days Patient´s (or relative´s if applicable) written informed consent Exclusion Criteria: Known sensitisation against the proposed antiseptics Tunneled or implanted CVCs (e.g. Hickman Catheter) Administration of antimicrobial drugs for therapy (not prophylaxis) less than one week prior to catheterization Pre-existing bloodstream infection (i.e., fever and/or other signs of infection) Positive blood culture Terminal patients with limited therapy options Patients with burns Patients participating in a clinical trial on other antiseptics within a period of four weeks prior to inclusion date Patients with missing written consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Markus Dettenkofer, Prof. MD
Organizational Affiliation
Institute of Environmental Medicine and Hospital Epidemiology University Medical Center Freiburg, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Environmental Medicine and Hospital Epidemiology University Medical Center Freiburg
City
Freiburg
Country
Germany
Facility Name
Division of Infectious Diseases and Hospital Epidemiology, University Hospital Basel
City
Basel
Country
Switzerland

12. IPD Sharing Statement

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Prevention of Catheter-Associated Infection With the Skin Disinfectant Octenidine Dihydrochloride

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