Viewing Study NCT02822768


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Study NCT ID: NCT02822768
Status: UNKNOWN
Last Update Posted: 2023-06-27
First Post: 2016-06-30
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Packing Versus no Packing for Cutaneous Abscess
Sponsor: University of California, San Francisco
Organization:

Study Overview

Official Title: Is Routine Packing of Cutaneous Abscesses Necessary?
Status: UNKNOWN
Status Verified Date: 2023-06
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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.
Detailed Description: Study protocol:

1. Identification of a patient with a cutaneous abscess requiring incision and drainage
2. Written consent obtained from the patient
3. 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

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: