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A Randomized Blinded Trial of Abscess Management With Packing vs No Packing

L

Lawson Health Research Institute

Status

Withdrawn

Conditions

Uncomplicated Cutaneous Abscess

Treatments

Procedure: Packing vs No Packing

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Adult patients presenting to the emergency department with superficial cutaneous abscesses will be randomized after incision and drainage to standard care with wound packing or no packing to determine if there is a difference in the proportion of complications between the two groups.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ≥ 18 years
  • Abscess ≤ 5cm in diameter
  • Truncal or extremity location

Exclusion criteria

  • Post-operative abscess (abscess in location of operative incision, operation within the last 4 months)
  • HIV/immunocompromised/transplant recipient/chronic oral steroid use
  • Fever at triage (temp ≥38 degrees Celsius)
  • Abscess secondary to Crohn's
  • Multiple abscesses requiring drainage
  • Prior participation in the study for the same abscess
  • Incision and drainage performed with no packing required, or where abscess cavity is <1 cm max diameter
  • Bartholins/perigenital, perianal, or facial abscesses
  • Complicated abscesses (fistula, suspicion of muscular extension, consultation/direct referral to general surgery)
  • Inability to give consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 2 patient groups

No Packing
Active Comparator group
Description:
No Packing
Treatment:
Procedure: Packing vs No Packing
Packing
Experimental group
Description:
Packing
Treatment:
Procedure: Packing vs No Packing

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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