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Abscess Cavity Packing for Skin Abscess
N/A
Recruiting
Led By Michael Darracq, MD, MPH
Research Sponsored by University of California, San Francisco
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients that require a cutaneous abscess incision and drainage
English-speaking subjects only
Must not have
Patients with infected bursa
Non-English speaking subjects
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 14 days
Summary
This trial is studying whether filling the space left after draining a skin infection helps patients heal better. It focuses on people with skin abscesses and aims to see if this method reduces the need for more treatments.
Who is the study for?
This trial is for English-speaking adults over 18 who need an abscess in their skin drained and can come back for a check-up in two days. It's not for pregnant women, minors, prisoners, those with infected bursa, non-English speakers, or patients needing hospital admission.
What is being tested?
The study is looking at whether putting gauze (packing) into the space where an abscess was after draining it affects the need for more treatments like another drainage procedure, antibiotics, or hospital stays.
What are the potential side effects?
Potential side effects may include discomfort from packing material in the wound site, possible delayed healing or infection due to packing presence or absence. Individual reactions to wound treatment will vary.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I need surgery to drain an abscess on my skin.
Select...
I speak English.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have an infection in the fluid-filled sac near my joint.
Select...
I do not speak English.
Select...
I am going to the hospital for surgery to drain an infection.
Select...
I cannot come back for a follow-up in 48 hours.
Select...
I am under 18 years old.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 14 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~14 days
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Percentage of patients needing further treatment
Secondary study objectives
Visual Analog Scale for Pain (VAS pain) post procedure
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: PackingActive Control1 Intervention
The patient is to have a long piece of gauze within the abscess cavity in an attempt to keep it open and allow purulent material to continue to drain after the initial incision and release of purulent material has been performed.
Group II: No packingPlacebo Group1 Intervention
The patient is not to have packing of the abscess as part of the incision and drainage procedure
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for skin abscesses include incision and drainage, often followed by packing the abscess cavity. The primary mechanism of action for incision and drainage is to physically remove pus and debris, reducing infection and pressure.
Packing the cavity with gauze or a silicone device helps maintain an open drainage pathway, preventing premature closure of the abscess and allowing continuous drainage of any residual infection. This is crucial for preventing recurrence and promoting proper healing.
These treatments are essential for skin abscess patients as they directly address the infection source and facilitate effective healing.
Randomized Controlled Trial of a Novel Silicone Device for the Packing of Cutaneous Abscesses in the Emergency Department: A Pilot Study.Volume-controlled vs no/short-term drainage after axillary lymph node dissection in breast cancer surgery: a meta-analysis.Negative pressure wound therapy: "a rose by any other name".
Randomized Controlled Trial of a Novel Silicone Device for the Packing of Cutaneous Abscesses in the Emergency Department: A Pilot Study.Volume-controlled vs no/short-term drainage after axillary lymph node dissection in breast cancer surgery: a meta-analysis.Negative pressure wound therapy: "a rose by any other name".
Find a Location
Who is running the clinical trial?
University of California, San FranciscoLead Sponsor
2,580 Previous Clinical Trials
15,177,304 Total Patients Enrolled
Michael Darracq, MD, MPHPrincipal InvestigatorUCSF - Fresno
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I speak English.I have an infection in the fluid-filled sac near my joint.I do not speak English.I am going to the hospital for surgery to drain an infection.I am 18 years old or older.I need surgery to drain an abscess on my skin.I cannot come back for a follow-up in 48 hours.I am under 18 years old.
Research Study Groups:
This trial has the following groups:- Group 1: Packing
- Group 2: No packing
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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