- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03036358
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 ED Setting
April 3, 2018 updated by: Benjamin Kaffenberger, Ohio State University
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.
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The Investigator hope to determine if the implementation of teledermatology in the emergency department (ED) at The Ohio State University Wexner Medical Center is beneficial in diagnosing cases of cellulitis and pseudocellulitis conditions.
Prior studies have indicated that misdiagnosis may occur in up to 28% of patients in the ED with these conditions.
Additionally, dermatological consults have been shown to change diagnosis or management of these conditions in more than 60% of the patients examined.
Without the use of teledermatology, however, a dermatological consult would be prohibitively expensive and take time to obtain.
The investigator proposes that by utilizing teledermatology in emergency rooms, the investigator can make faster, yet just as accurate, dermatological diagnoses in patients presenting with cellulitis-like symptoms.
Subsequently, by reducing the number of misdiagnoses, unnecessary use of antibiotics and hospitalizations will also decrease, lowering health care costs and simultaneously providing patients with faster treatment of the actual dermatologic condition.
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ohio
-
Columbus, Ohio, United States, 43210
- The Ohio State University Wexner Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Over 18
- Present to the ED with cellulitis-like symptoms, including but not limited to the following: tenderness, redness, swelling, expansive lesion
Exclusion Criteria:
- pregnant
- prisoner
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Teledermatology consult
To determine the benefit of teledermatology to differentiate cellulitis from pseudocellulitis in emergency departments through the analysis of time spent in the emergency department (ED), admission to the inpatient hospital, antibiotic use, time to improvement, and 30-day remission rate.
This arm will undergo imaging, a dermatologic assessment will be performed, AND this assessment will be entered into the patients chart.
|
Information from the dermatologic assessment will be entered into the patients chart.
|
Other: Routine Care
To determine the benefit of teledermatology to differentiate cellulitis from pseudocellulitis in emergency departments through the analysis of time spent in the emergency department (ED), admission to the inpatient hospital, antibiotic use, time to improvement, and 30-day remission rate.
This arm will undergo imaging, a dermatologic assessment will be performed, AND this assessment WILL NOT be entered into the patients chart
|
The dermatologic assessment will occur but not added to the patients medical record.
Dermatology may still be consulted but will be at the prerogative of the treating hospitalist.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Admission to the hospital
Time Frame: 30 days
|
To determine the benefit of teledermatology to differentiate cellulitis from pseudocellulitis in emergency departments through the analysis of time spent in the emergency department (ED), admission to the inpatient hospital, antibiotic use, time to improvement, We anticipate a high rate of pseudocellulitis, and this aim will determine if there is a difference in patient admissions among those who receive a dermatologic assessment
|
30 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Length of stay in the hospital
Time Frame: 30 days post admission
|
Will assess time spent in the hospital for those that were admitted
|
30 days post admission
|
30 day readmission rate
Time Frame: 30 days post admission
|
Will assess hospitalization/emergency department readmission in the following 30 days
|
30 days post admission
|
Antibiotic use
Time Frame: 30 days post admission
|
Will assess the frequency of antibiotic use between groups
|
30 days post admission
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2016
Primary Completion (Actual)
January 1, 2018
Study Completion (Actual)
January 1, 2018
Study Registration Dates
First Submitted
June 4, 2016
First Submitted That Met QC Criteria
January 26, 2017
First Posted (Estimate)
January 30, 2017
Study Record Updates
Last Update Posted (Actual)
April 5, 2018
Last Update Submitted That Met QC Criteria
April 3, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2015H0134
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Cellulitis
-
McGill University Health Centre/Research Institute...CompletedCellulitis | Cellulitis of Leg | Cellulitis of ArmCanada
-
University of SouthamptonUniversity of Nottingham; Norfolk and Norwich University Hospitals NHS Foundation... and other collaboratorsNot yet recruitingCellulitis of Leg
-
Hillel Yaffe Medical CenterUnknown
-
Lawson Health Research InstituteUniversity of Western Ontario, CanadaCompletedUncomplicated Outpatient CellulitisCanada
-
University of SussexCompletedCellulitis | Cellulitis of Leg | Antibiotic DurationUnited Kingdom
-
University Hospital Plymouth NHS TrustTerminated
-
BTL Industries Ltd.CompletedCellulitis | Cellulite | Cellulitis of LegUnited States
-
InMode MD Ltd.RecruitingCellulitis of LegUnited States
-
Cairo UniversityRecruitingFibrosis | Lower Limb Lymphedema | Cellulitis of LegEgypt
-
Minia UniversityCompletedEndophthalmitis and Orbital CellulitisEgypt
Clinical Trials on teledermatology consult
-
Ohio State UniversityCompleted
-
US Department of Veterans AffairsCompletedSkin Diseases | Quality of Life | TelemedicineUnited States
-
University Paris 7 - Denis DiderotCompletedDermatologic ConditionsFrance
-
US Department of Veterans AffairsCompleted
-
NYU Langone HealthThe Rainer Arnhold FoundationCompletedCoronary Artery Disease | Hypertension | Obesity | Diabetes | Peripheral Arterial Disease | Hyperlipidemia | PrediabetesUnited States
-
University of VermontNeurocrine BiosciencesRecruitingDrug-Induced Movement DisorderUnited States
-
Radboud University Medical CenterUnknown
-
VA Office of Research and DevelopmentVA Boston Healthcare System; Durham VA Health Care System; Providence VA Medical...RecruitingNew Patient Use of Teledermatology Mobile AppUnited States
-
Turtle Health, Inc.WithdrawnFertility RiskUnited States
-
University of VirginiaNamrita OdackalCompletedPremature Birth | Prenatal StressUnited States