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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00875069
Other study ID # CHU-0050
Secondary ID
Status Completed
Phase Phase 3
First received April 2, 2009
Last updated June 13, 2014
Start date April 2009
Est. completion date February 2013

Study information

Verified date June 2014
Source University Hospital, Clermont-Ferrand
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

The primary objective of the study is to demonstrate the efficacy of 60% ethanol lock solution in preventing major catheter related infections in critically ill patients.


Description:

The primary objective of the study is to demonstrate the efficacy of 60% ethanol lock solution in preventing major catheter related infections in critically ill patients


Recruitment information / eligibility

Status Completed
Enrollment 1460
Est. completion date February 2013
Est. primary completion date June 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients of both genders, over 18 years,

- Patients admitted in ICU

- Dialysis catheter insertion for renal replacement therapy

- At least two renal replacement therapy sessions

- Written informed consent

- Social security

Exclusion Criteria:

- Pregnant or breastfeeding women

- Patient requiring dialysis on arteriovenous fistula or permanent catheter

- Known allergy to ethanol

- Dialysis catheter covered or impregnated with antimicrobial agent

- Dialysis catheter insertion before ICU admission

- Single-lumen dialysis catheters

- Patient whose death is likely to occur within hours after admission to ICU

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)


Intervention

Other:
Ethanol
Dialysis catheter lock performed after renal replacement therapy session. Lock is instilling ethanol (or placebo) in each catheter lumen for 2 minutes before being withdrawn.

Locations

Country Name City State
France CHU Clermont-Ferrand Clermont-Ferrand

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Clermont-Ferrand

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary The number of major catheter-related infections (CRI) defined as either catheter-related clinical sepsis without bloodstream infection or catheter-related bloodstream infection (CRBSI), during the ICU stay after renal replacement therapy session Yes
Secondary frequencies of catheter colonization, severe mechanical complications, and adverse events for two minutes before being withdrawn Yes
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