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Utility of Trimethoprim-sulfamethoxazole Use in Skin Abscess Management

Primary Purpose

Skin Diseases, Infectious

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Trimethoprim-sulfamethoxazole
Placebo group
Sponsored by
St. Louis University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Skin Diseases, Infectious focused on measuring skin abscess, CA-MRSA

Eligibility Criteria

3 Months - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • non-toxic patients
  • immunocompetent patients
  • 3 months to 18 years old
  • English-speaking patients
  • skin abscesses
  • not on antibiotics

Exclusion Criteria:

  • toxic patients
  • immunocompromising co-morbidities
  • less than 3 months old or older than 18 years of age
  • non-english speaking
  • on antibiotics

Sites / Locations

  • Cardinal Glennon Children's Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

placebo group

antibiotic group

Arm Description

Maalox and bitter mixture

Trimethoprim-sulfamethoxazole suspension

Outcomes

Primary Outcome Measures

Skin Abscess Resolution

Secondary Outcome Measures

New Lesion Development and Spread of Skin Abscesses (on Subject)
The secondary outcomes of interest included the development of new lesions at a different site (>5cm away from original skin abscess) on day 10 clinical follow-up or self-report and 3 month telephone follow-up.

Full Information

First Posted
May 14, 2008
Last Updated
April 2, 2018
Sponsor
St. Louis University
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1. Study Identification

Unique Protocol Identification Number
NCT00679302
Brief Title
Utility of Trimethoprim-sulfamethoxazole Use in Skin Abscess Management
Official Title
A Double Blinded Randomized Controlled Trial for the Management of Pediatric Community Acquired Skin Abscesses - To Treat or Not to Treat With Antibiotics
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
July 2006 (undefined)
Primary Completion Date
February 2008 (Actual)
Study Completion Date
May 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St. Louis University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if antibiotics are required in the management of skin abscess following incision and drainage.
Detailed Description
This is a double-blind, randomized controlled trial at an urban pediatric emergency department. Sample size (162) was based on a threshold equivalence of 7% (α = 0.05, power = 80%). Inclusion criteria were: non-toxic, immunocompetent, 3 months to 18 years old, English-speaking patients with clinical or ultrasound identified skin abscesses who were not on antibiotics. Patients were block randomized to receive placebo or trimethoprim/sulfamethoxazole following incision and drainage. Follow-up was a call at 2-3 days & a repeat visit or call at 10-14 days. Treatment failure was defined as: persistent erythema, tenderness, and/or draining lesions. New lesion was defined as: primary resolution with development of new lesion (furuncle, carbuncle or abscess) at a different location. Compliance was evaluated by the return of the study medication or by patient report.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Skin Diseases, Infectious
Keywords
skin abscess, CA-MRSA

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
161 (Actual)

8. Arms, Groups, and Interventions

Arm Title
placebo group
Arm Type
Placebo Comparator
Arm Description
Maalox and bitter mixture
Arm Title
antibiotic group
Arm Type
Active Comparator
Arm Description
Trimethoprim-sulfamethoxazole suspension
Intervention Type
Drug
Intervention Name(s)
Trimethoprim-sulfamethoxazole
Other Intervention Name(s)
Septra
Intervention Description
Participants were randomized to receive placebo or trimethoprim/sulfamethoxazole using a computer randomization program on the initial presentation. The placebo is a Maalox and tonic water combination that resembled the antibiotic in color, texture and taste. The antibiotic dose is a standard trimethoprim/sulfamethoxazole for bacterial infection (10-12mg trimethoprim/kg/day, with a maximum adult dose of 160mg trimethoprim/day, divided into two doses). The concentration of the liquid is 200mg sulfamethoxazole/40mg trimethoprim per 5mL. With a maximum dose of 160mg trimethoprim, this equates to 20mL.
Intervention Type
Drug
Intervention Name(s)
Placebo group
Other Intervention Name(s)
Maalox (with simethicone and bitter mixture)
Intervention Description
Placebo (Maalox with simethicone and bitter mixture) suspension was dispensed to study participants who were block randomized to receive the placebo.
Primary Outcome Measure Information:
Title
Skin Abscess Resolution
Time Frame
10-14 days
Secondary Outcome Measure Information:
Title
New Lesion Development and Spread of Skin Abscesses (on Subject)
Description
The secondary outcomes of interest included the development of new lesions at a different site (>5cm away from original skin abscess) on day 10 clinical follow-up or self-report and 3 month telephone follow-up.
Time Frame
10-14 days and 3 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Months
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: non-toxic patients immunocompetent patients 3 months to 18 years old English-speaking patients skin abscesses not on antibiotics Exclusion Criteria: toxic patients immunocompromising co-morbidities less than 3 months old or older than 18 years of age non-english speaking on antibiotics
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Peter, MD
Organizational Affiliation
St. Louis University
Official's Role
Study Director
Facility Information:
Facility Name
Cardinal Glennon Children's Medical Center
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18222564
Citation
Pallin DJ, Egan DJ, Pelletier AJ, Espinola JA, Hooper DC, Camargo CA Jr. Increased US emergency department visits for skin and soft tissue infections, and changes in antibiotic choices, during the emergence of community-associated methicillin-resistant Staphylococcus aureus. Ann Emerg Med. 2008 Mar;51(3):291-8. doi: 10.1016/j.annemergmed.2007.12.004. Epub 2008 Jan 28.
Results Reference
background
PubMed Identifier
17934031
Citation
Korownyk C, Allan GM. Evidence-based approach to abscess management. Can Fam Physician. 2007 Oct;53(10):1680-4.
Results Reference
background
PubMed Identifier
17902728
Citation
Cohen PR. Community-acquired methicillin-resistant Staphylococcus aureus skin infections: implications for patients and practitioners. Am J Clin Dermatol. 2007;8(5):259-70. doi: 10.2165/00128071-200708050-00001.
Results Reference
background
PubMed Identifier
14872177
Citation
Lee MC, Rios AM, Aten MF, Mejias A, Cavuoti D, McCracken GH Jr, Hardy RD. Management and outcome of children with skin and soft tissue abscesses caused by community-acquired methicillin-resistant Staphylococcus aureus. Pediatr Infect Dis J. 2004 Feb;23(2):123-7. doi: 10.1097/01.inf.0000109288.06912.21.
Results Reference
background
PubMed Identifier
19409657
Citation
Duong M, Markwell S, Peter J, Barenkamp S. Randomized, controlled trial of antibiotics in the management of community-acquired skin abscesses in the pediatric patient. Ann Emerg Med. 2010 May;55(5):401-7. doi: 10.1016/j.annemergmed.2009.03.014. Epub 2009 May 5.
Results Reference
derived

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Utility of Trimethoprim-sulfamethoxazole Use in Skin Abscess Management

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