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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01148030
Other study ID # 11319
Secondary ID
Status Terminated
Phase Phase 4
First received June 18, 2010
Last updated February 28, 2014
Start date June 2010
Est. completion date July 2012

Study information

Verified date February 2014
Source 3M
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Patients presenting in the Emergency Department or admitted to the hospital with displaced hip fractures who require hemiarthroplasty or open reduction internal fixation or with spinal instability/fractures in need of urgent surgical intervention will receive treatment to reduce the number of microorganisms in their nose prior to surgery. After surgery, the subjects will be observed for any surgical site infections.


Description:

Infection rate study.


Recruitment information / eligibility

Status Terminated
Enrollment 333
Est. completion date July 2012
Est. primary completion date July 2012
Accepts healthy volunteers No
Gender Both
Age group 2 Years and older
Eligibility Inclusion Criteria:

- Patients presenting in the Emergency Department or admitted to the hospital with displaced hip fractures who require hemiarthroplasty or open reduction internal fixation or with spinal instability/fractures in need of urgent surgical intervention will be enrolled in the study.

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Drug:
3M Skin and Nasal Antiseptic
Intra-nasal dosing

Locations

Country Name City State
United States Sharp Memorial Hospital San Diego California

Sponsors (2)

Lead Sponsor Collaborator
3M Sharp HealthCare

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Surgical Site Infection 1 year after surgery No
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