Potential Nosocomial Infection Prevention Via Modification of Anesthesia Intraoperative Aseptic Practice
NCT ID: NCT00617006
Last Updated: 2008-02-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
114 participants
OBSERVATIONAL
2007-07-31
2007-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Hand Hygiene and Hospital Acquired Infections
NCT02252562
Evaluation of Body-worn Multimodal Hand Hygiene System. Impact on Health-Care Associated Infections
NCT01050608
Bacterial Contamination of Anaesthetists' Hands by Personal Mobile Phones Used in the Operating Theatre
NCT00416936
Efficacy of CHX Cloths Versus CHX Soaps for Bathes Before Orthopedic Surgery
NCT05120739
Prospective, Randomized Study Evaluating The Efficacy of Chlorhexidine Gluconate Impregnated No-Rinse Cloths.
NCT02469311
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
ECOLOGIC_OR_COMMUNITY
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Before (Control)
Study group representative of standard practice
No interventions assigned to this group
After(Treatment)
After treatment group with the personal hand hygiene device ie. Device Group.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Harbor Medical Inc.
INDUSTRY
Dartmouth-Hitchcock Medical Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dartmouth-Hitchcock Medical Center
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Matthew D Koff, M.D. M.S.
Role: PRINCIPAL_INVESTIGATOR
Dartmouth-Hitchocck Medical Center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Dartmouth-Hitchcock Medical Center
Lebanon, New Hampshire, United States
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Koff MD, Loftus RW, Burchman CC, Schwartzman JD, Read ME, Henry ES, Beach ML. Reduction in intraoperative bacterial contamination of peripheral intravenous tubing through the use of a novel device. Anesthesiology. 2009 May;110(5):978-85. doi: 10.1097/ALN.0b013e3181a06ec3.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CPHS# 20655
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.