Pneumonia Clinical Trial
Official title:
Effect of Topical Oral Chlorhexidine in Reducing Pneumonia in Nursing Home Residents
Verified date | December 2016 |
Source | University of Louisville |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is determine if topical oral application of a chlorhexidine antimicrobial spray will significantly reduce pneumonia and respiratory infections, and improve oral health compared to a placebo solution in nursing home residents.
Status | Completed |
Enrollment | 75 |
Est. completion date | July 2011 |
Est. primary completion date | July 2011 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 65 Years and older |
Eligibility |
Inclusion Criteria: 1. Participants must be at least 65 years old. 2. Be dependent in 2 or more Activities of Daily Living as noted on the nursing home resident's Minimum Data Set - One must be ADL J- Personal Hygiene. 3. Have natural teeth and/or wear complete or partial dentures. 4. Expected to be a resident in a nursing home for two years. Exclusion Criteria: 1. Existing pneumonia. 2. History of chlorhexidine reaction or allergy and/or multiple medication or substance allergies. 3. Receiving chlorhexidine oral application at enrollment as prescribed by physician or dentist. |
Country | Name | City | State |
---|---|---|---|
United States | University of Louisville | Louisville | Kentucky |
Lead Sponsor | Collaborator |
---|---|
University of Louisville | National Institute of Dental and Craniofacial Research (NIDCR) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pneumonia | 12 months | ||
Secondary | Respiratory pathogens | 12 months | ||
Secondary | Plaque and Gingival Indices | 12 months |
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