Cellulitis Clinical Trial
Official title:
Handheld Infrared Thermometer to Evaluate Cellulitis
It can be difficult to differentiate cellulitis from non-infectious mimics, like venous
stasis. One way of determining the difference is feeling skin surface temperature. However,
this is a subjective measure that is inherently unreliable. It might be possible to objectify
this measurement by using a non-contact infrared thermometer at the bedside.
The goal of this study is therefore to assess whether objective difference in skin surface
temperature in an area of suspected cellulitis, relative to non-affected skin, has diagnostic
utility. It will use the diagnosis of cellulitis by an infectious diseases physician as the
gold standard and compare blinded temperature difference between affected and unaffected
limbs to that standard. It is hypothesized that measurement of skin surface temperature by
non-contact infrared thermometer will help differentiate cellulitis from many non-infectious
conditions that mimic cellulitis.
For patients who are hospitalized, the study also plans to see whether a change in this
temperature difference is predictive of response to treatment when compared to the FDA
standard for early response and patient reported symptoms.
This is a pragmatic, prospective cohort study. Patients with suspected cellulitis who receive
an infectious diseases consult (in the emergency room or urgent clinic) will be approached
for consent and enrollment. The goal is to enroll approximately 50 patients with a minimum of
10-15 cases of non-cellulitis.
These measurements will not be made available to the treating teams. This is an observational
study only comparing the potential value of these measurements to usual clinical care.
n/a
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02864420 -
Hospitalization at Home: The Acute Care Home Hospital Program for Adults
|
N/A | |
Completed |
NCT00746109 -
Study of Wound Packing After Superficial Skin Abscess Drainage
|
Phase 4 | |
Completed |
NCT03296280 -
Evaluation of Implementation of a National Point-of-Care Ultrasound Training Program
|
||
Completed |
NCT01876628 -
Adjunctive Clindamycin for Cellulitis: C4C Trial.
|
Phase 4 | |
Not yet recruiting |
NCT01947660 -
Continuous Regional Anesthesia for Septic Limb Orthopedic Surgery
|
N/A | |
Active, not recruiting |
NCT01706913 -
Study Assessing Impact of Dermatology Consultation for Patients Admitted With Cellulitis
|
N/A | |
Completed |
NCT03474523 -
Effectiveness of Diathermy-Radiofrecuency Compared With Cavitation in Cellulitis Treatment
|
N/A | |
Recruiting |
NCT03312946 -
Effect of Vibro-oscillatory Therapy for Improvement of Body Contour and Appearance of Cellulite.
|
N/A | |
Active, not recruiting |
NCT05226260 -
Decreasing Antibiotic Duration for Skin and Soft Tissue Infection Using Behavioral Economics in Primary Care
|
N/A | |
Active, not recruiting |
NCT03785834 -
The Effect of Histopathologic Analysis and Tissue Cultures on Inpatient Management of Cellulitis and Pseudocellulitis
|
||
Completed |
NCT01549613 -
Evaluation of Daptomycin for the Emergency Department Treatment of Complicated Skin and Skin Structure Infections
|
Phase 4 | |
Completed |
NCT01029782 -
Comparison of Intravenous Cefazolin Plus Oral Probenecid With Oral Cephalexin for the Treatment of Cellulitis
|
Phase 2 | |
Completed |
NCT00676130 -
Study of New Antibiotic Regimen for the Treatment of Uncomplicated Cellulitis in Emergency Department Patients
|
N/A | |
Not yet recruiting |
NCT03917134 -
Prevention of Vaginal Cellulitis or Vaginal Cuff Abscess After Laparoscopic Hysterectomy
|
N/A | |
Completed |
NCT02230813 -
Predictors of Oral Antibiotic Treatment Failure in Emergency Department Patients With Cellulitis
|
N/A | |
Completed |
NCT01557426 -
Soft Tissue Ultrasound of Infections
|
Phase 1 | |
Completed |
NCT01339091 -
Efficacy and Safety of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections
|
Phase 3 | |
Completed |
NCT00984022 -
Aquacel Versus Iodoform Gauze for Filling Abscess Cavity Following Incision and Drainage
|
Phase 2 | |
Completed |
NCT04091672 -
RECELL® System Combined With Meshed Autograft for Reduction of Donor Skin Harvesting in Soft Tissue Reconstruction
|
N/A | |
Completed |
NCT05023200 -
The Personalised Antibiotic Duration for Cellulitis (PAD-C) Study
|