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Potential Nosocomial Infection Prevention Via Modification of Anesthesia Intraoperative Aseptic Practice

Before and After Study Evaluating Deployment of the Sprixx GJ Personal Hand Hygiene Device in the Intra-Operative Environment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00617006
Enrollment
114
Registered
2008-02-15
Start date
2007-07-31
Completion date
2007-10-31
Last updated
2008-02-15

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

Conditions

Nosocomial Infections

Keywords

Anesthesia Workspace, Hospital Acquired Infections, Hand Hygiene, Alcohol Based Cleanser, Bacterial Contamination

Brief summary

We hypothesized that by improving hand hygiene compliance in the operative environment, we would reduce horizontal transmission of pathogenic bacteria to surgical patients.

Detailed description

We performed an observational study evaluating provider adherence to these techniques. We then sought to increase hand hygiene compliance through the use of a point of care alcohol based hand hygiene device. We hypothesized that increased hand hygiene compliance would reduce bacterial contamination of the anesthesia workspace and peripheral intravenous tubing, and ultimately reducing overall morbidity and mortality secondary to a reduction in nosocomial infection rates.

Interventions

None listed

Sponsors

Harbor Medical Inc.
CollaboratorINDUSTRY
Dartmouth-Hitchcock Medical Center
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients present in operating rooms randomized to study.

Exclusion criteria

* Patients that were already enrolled in study and return to the operating room.

Design outcomes

Primary

MeasureTime frame
The presence of a positive culture on the previously sterile patient stopcock set, and the presence of multidrug resistant bacteriaBeginning and end of surgical case

Secondary

MeasureTime frame
Reduction of bacterial contamination on predetermined sites on the anesthesia machineBeginning and End of Surgical Case
Decreased length of stayPostoperatively
Nosocomial infection rateswithin 30 days postoperatively
MortalityWithin 30 days postoperatively

Countries

United States

Outcome results

None listed

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