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OpenTrials
Recruiting

NCT Number: NCT02822768

Packing Versus no Packing for Cutaneous Abscess

The goal of this study is to examine patients undergoing incision and drainage of cutaneous abscesses to determine if routine packing of the abscess cavity affects the need for further interventions such as repeat incision and drainage, antibiotic administration or hospital admission.

Recruiting

Interested in participating?

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Study protocol:

  • Identification of a patient with a cutaneous abscess requiring incision and drainage
  • Written consent obtained from the patient
  • Study materials will be obtained
  • Enrolling physician fills out pre-procedure information (see data sheet)
  • Enrollment data sheet has instructions indicating whether patient is to receive packing or not
  • Use of random number generator to randomize all packets
  • Provider does abscess incision and drainage with or without packing according to the instructions
  • Enrolling physician fills out post-procedure information (see data sheet)
  • Patient returns within 48 hours for wound check with removal of packing if performed
  • Research coordinator or study physician calls the patient within 14 and 30 days after the procedure for follow-up
  • Information from a return visit and/or the telephone follow-up

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients 18 years of age and above
  • Patients that require a cutaneous abscess incision and drainage
  • English-speaking subjects only

Exclusion criteria

  • Unable to return for 48-hour follow-up.
  • Patients being admitted to the hospital or going to the operating room for incision and drainage
  • Pregnant patients
  • Patients less than 18 years of age
  • Prisoners or persons in police custody
  • Patients with infected bursa
  • Non-English speaking subjects

Treatment and study plan

Packing

Procedure

The patient will receive packing as part of their wound care

No packing

Other

The patient will not receive packing as part of their wound care

Primary outcomes

  1. Percentage of patients needing further treatment

    Time frame: 14 days

    follow-up call to determine if patient required further treatment beyond routine care

Secondary outcomes

  1. Visual Analog Scale for Pain (VAS pain) post procedure

    Time frame: 14 days

    Measure pain score after procedure

Study contacts

Contact information is provided by the study sponsor or research team.

Jannet Castaneda, BA

CONTACT

[email protected]

559-499-6435

Michael Darracq, MD, MPH

CONTACT

[email protected]

559-499-6440

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Registry information

Official study title

Is Routine Packing of Cutaneous Abscesses Necessary?

Important dates

Study start
2016
Primary completion
2026
Study completion
2026
First posted
Jul 4, 2016
Registry last updated
Jan 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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