Study Comparing CUBICIN® (Daptomycin for Injection) With Vancomycin in Cellulitis or Erysipelas



Status:Completed
Conditions:Cosmetic
Therapuetic Areas:Dermatology / Plastic Surgery
Healthy:No
Age Range:18 - Any
Updated:9/8/2017
Start Date:February 20, 2006
End Date:August 9, 2006

Use our guide to learn which trials are right for you!

A Multicenter, Randomized Study Comparing CUBICIN® (Daptomycin for Injection) With Vancomycin in the Treatment of Cellulitis or Erysipelas

This study is designed to investigate the difference in speed and degree of symptom
resolution between daptomycin and vancomycin in subjects treated for cellulitis or erysipelas
by evaluation of the following parameters:

- Time to erythema margin cessation to progress

- Time to defervescence

- Time to hospital discharge following relief of the presenting cellulitis or erysipelas

- Degree of improvement of the following signs and symptom of cellulitis or erysipelas
including

- Degree of improvement of cellulitis-related pain and swelling as reported by subjects

Additionally, the difference in frequency of Adverse Events between daptomycin and vancomycin
will be described.

same as above

Inclusion Criteria:

1. Read and sign the informed consent form after the nature of the study has been fully
explained;

2. Male or female > or = 18 years of age;

3. If female of childbearing potential, a negative pregnancy test is required;

4. Primary diagnosis of cellulitis/ erysipelas

1. with onset of signs or symptoms within 3 days of 1st dose of study medication

2. requiring hospitalization, and severe enough to warrant IV antibiotics

3. temperature >37.5°C (99.5° F) oral or >38° C (100.2° F) rectal, documented within
48 hours prior to enrollment, and

4. anticipated treatment to be limited to medical (NOT surgical) interventions

5. at an anatomical location that allows of a clear assessment of the erythema
margin

Exclusion Criteria:

1. Pregnant or lactating female;

2. Conditions where required surgery (in and of itself) constitutes curative treatment of
the infection or removal of infected site (e.g., amputation);

3. Conditions requiring emergent surgical intervention at the site of infection (e.g.,
progressive necrotizing infections);

4. Previous systemic antimicrobial therapy exceeding 24 hours duration, administered
anytime during the 72 hours prior to the first dose of study drug unless on previous
antibiotics for at least 72 hours and without any clinical improvement;

5. Cellulitis associated with a wound infection or ulcer requiring incision and drainage
or debridement

6. Perirectal abscess or hidradenitis suppurativa or third degree burn infections

7. Buccal cellulitis, facial cellulitis, perianal cellulitis, or periorbital cellulitis;

8. Known or suspected osteomyelitis, pneumonia, bacteremia, endocarditis, or urinary
tract infection;

9. Known to be allergic or intolerant to study medications;

10. Subjects with a Creatinine Clearance (CLCR) <30 mL/min;

11. Requirement for non-study systemic antibiotics;

12. Requirement for systemic steroids from enrollment through stabilization of cellulitis;

13. Rhabdomyolysis;

14. Neutropenic subjects with absolute neutrophil count ≤ 500 cells/mm3
We found this trial at
1
site
3675 J Dewey Gray Circle
Augusta, Georgia 30909
?
mi
from
Augusta, GA
Click here to add this to my saved trials