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NCT03034694 Clinical Trial

The Effect of Dermatology and Teledermatology Consultations on Length of Hospital Admission, 30 Day Readmission Rate, and Antibiotic Use in Patients Presenting With Cellulitis vs Pseudocellulitis in an Academic Inpatient Setting

Cellulitis Clinical Trial

Official title:
The Effect of Dermatology and Teledermatology Consultations on Length of Hospital Admission, 30 Day Readmission Rate, and Antibiotic Use in Patients Presenting With Cellulitis vs Pseudocellulitis in an Academic Inpatient Setting

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03034694
Other study ID # 2015H0393
Secondary ID
Status Completed
Phase N/A
First received June 4, 2016
Last updated January 16, 2018
Start date January 2016
Est. completion date January 2018

Study information
Verified date January 2018
Source Ohio State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The effect of teledermatology on length of hospital admission, length of stay, 30 day readmission rate, and antibiotic use in patients presenting with cellulitis vs pseudocellulitis in an academic emergency department setting.

Recruitment information / eligibility
Status Completed
Enrollment 45
Est. completion date January 2018
Est. primary completion date January 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Over 18

- Admission for cellulitis-like symptoms, including but not limited to the following: tenderness, redness, swelling, expansive lesion

Exclusion Criteria:

- pregnant

- prisoner

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• teledermatology consult
teledermatology consult
• Routine Care
The patient will undergo imaging but this report will not be put into the chart.

Locations
Country Name City State
United States The Ohio State University Wexner Medical Center Columbus Ohio

Sponsors (1)
Lead Sponsor Collaborator
Ohio State University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Length of Hospitalization 60 Days
Secondary Readmission rate 30 Days
Secondary Frequency/Use of antibiotics 30 days
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