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NCT00713674 Clinical Trial

Comparison of Decolonization of Methicillin-resistant Staphylococcus Aureus (MRSA) Using Theraworx

Methicillin-Resistant Staphylococcus Aureus Clinical Trial

— SJMRSA  

Official title:
Comparison of Decolonization of MRSA Using Theraworx

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00713674
Other study ID # SJMRSA-01
Secondary ID
Status Withdrawn
Phase N/A
First received July 7, 2008
Last updated March 21, 2017
Start date March 2008
Est. completion date February 2009

Study information
Verified date March 2017
Source Mercy Research
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to examine treatment method of Methicillin-resistant Staphylococcus aureus (MRSA) decolonization in patients.

Description:

Decolonization therapy is indicated for management of patients with MRSA. Theraworx is reported to be an effective antimicrobial against multiple organisms. In this study, patients with positive MRSA colonization culture will be treated with Theraworx to evaluate decolonization duration capability.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date February 2009
Est. primary completion date February 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Positive MRSA culture

Exclusion Criteria:

- Patients currently on or start antibiotic therapy directed for MRSA.(Prophylaxis antibiotic for surgical procedure not considered therapy.)

- Patients with MRSA infected wounds

- Patients under the age of 18 years

- A woman currently pregnant or nursing a child

- Patients participating in another study within 30 days of randomization

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Theraworx
Theraworx swab intranasal BID for 5 days
Drug:
• mupirocin antibiotic ointment
mupirocin antibiotic ointment swab intranasal BID for 5 days

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Mercy Research

Outcome
Type Measure Description Time frame Safety issue
Primary Evidence of decolonization confirmed by intranasal culture Up to 14 days post treatment (+/- 1-2 days)
Secondary Economic-Cost comparison of treatment Evidence of decolonization 5 days of treatment
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