Abscess Packing Versus Wick Placement After Incision and Drainage

Sponsor
Washington University School of Medicine (Other)
Overall Status
Completed
CT.gov ID
NCT01281930
Collaborator
(none)
156
1
2
77
2

Study Details

Study Description

Brief Summary

Abscesses or "boils" are becoming more common every year and are a common reason children come to the Emergency Department. For the abscess to heal the skin needs to be opened to let the pus come out. Often doctors put something called "packing material" or gauze into the abscess space to help aid in healing. It is not known if the type of "packing" that is done is necessary or if a more simple treatment is as good or better. With informed consent we randomly place a child into one (1) of two (2) groups in this study that will say if the child's abscess/boil is packed with gauze in the traditional way or if a wick (small piece) of gauze is placed after the abscess/boil is opened and the fluid is drained. After treatment in the emergency department the child will be scheduled to follow-up in the Pediatric Acute Wound Service (PAWS) clinic as all other children with this infection are scheduled. At this visit the healing of the wound will be checked by the staff in the clinic and will be scored. With this evaluation of the wound the hypothesis that for a simple superficial (skin) abscess/boil a gauze wick placement into the abscess/boil is as effective as placement of traditional gauze packing.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Full packing into abscess cavity
  • Procedure: Wick placement into abscess cavity
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
156 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Abscess Packing Versus Wick Placement After Incision and Drainage
Study Start Date :
Jun 1, 2009
Actual Primary Completion Date :
Nov 1, 2015
Actual Study Completion Date :
Nov 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Wick placement into abscess cavity

Procedure: Wick placement into abscess cavity
After incision and drainage of the abscess a piece of plain gauze 1/4-1 inch packing material that is as wide as can be easily passed through the opening is placed into the cavity spanning one diameter of the cavity

Active Comparator: Full packing of abscess cavity

Procedure: Full packing into abscess cavity
After incision and drainage plain 1/4-1/2 inch gauze packing material is placed into the cavity to fill it

Outcome Measures

Primary Outcome Measures

  1. Abscess healing based upon clinical criteria and clinical judgement [24-72 hours]

    Abscesses are assessed for pus accumulation, erythema from the wound, if the patient has a fever and the overall clinical judgment of the evaluating health care professional at the time of follow-up.

Secondary Outcome Measures

  1. Pain since abscess drainage [24-72 hours]

  2. Parent/guardian comfort with removing the packing material or wick from the abscess cavity [24-72 hours]

  3. Parent/guardian assessment of the abscess wound at 2 weeks [2 weeks]

  4. Parent/guardian assessment of pus drainage at 2 weeks [2 weeks]

  5. Need for further treatment of same abscess within 2 weeks [2 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Months to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Well appearing patient

  • Abscesses restricted to the superficial areas of the extremities, buttocks, abdominal and thoracic walls, and back

  • Patients presenting Saturday-Wednesday

Exclusion Criteria:
  • Fever >38 degrees celsius

  • Ill appearing patient

  • Underlying immunodeficiency or disorder leading to chronic abscess formation

  • Any reason for admission to hospital beyond the need for sedation at the time of follow-up

  • Thursday-Friday

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. Louis Children's Hospital Saint Louis Missouri United States 63110

Sponsors and Collaborators

  • Washington University School of Medicine

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Washington University School of Medicine
ClinicalTrials.gov Identifier:
NCT01281930
Other Study ID Numbers:
  • 09-0719 -201103241
First Posted:
Jan 24, 2011
Last Update Posted:
Jun 19, 2018
Last Verified:
Jun 1, 2018
Keywords provided by Washington University School of Medicine
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 19, 2018