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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02286479
Other study ID # KOU KAEK 2014/259
Secondary ID
Status Completed
Phase N/A
First received November 5, 2014
Last updated August 12, 2016
Start date October 2014
Est. completion date August 2016

Study information

Verified date August 2016
Source Kocaeli University
Contact n/a
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Interventional

Clinical Trial Summary

Skin abscesses are among the most common soft tissue infections cause emergency room visits frequently. Management of abscess drainage and prevent further complications are important entities for emergency physicians. Historically primary incision and drainage (I&D) technique has found very effective method of abscess drainage, however a novel technique loop drainage holds promising. The purpose of our study is comparison efficacy of I&D and loop drainage techniques in patients with cutaneous abscess.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date August 2016
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patients presenting to Kocaeli University Emergency Department with cutaneous abscess.

- Providing written informed consent.

Exclusion Criteria:

- Under 18 years of age.

- Immunosuppressive patients.

- Using medications have effects on wound healing.

- Abscess is not recognizable by bedside ultrasound.

- Lidocaine allergy

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Incision and Drainage
In the incision and drainage group, the abscesses are incised, irrigated by sterile solutions and drained conventionally.
Loop drainage
In the loop drainage group, two small incision are made on each side of abscess. The pus are drained and septations are seperated by a forceps. Abscess cavitary irrigated by sterile solution. Sterile, non-powder, non-latex surgical gloves cuff is inserted in one incision and taken out from the other insicion. Then two tips of cuff are tied loosely.

Locations

Country Name City State
Turkey Kocaeli University Medical Faculty Emergency Medicine Department Kocaeli

Sponsors (1)

Lead Sponsor Collaborator
Kocaeli University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Other Procedure Pain Intensity intraoperative No
Primary Abscess Resolution 7 days No
Secondary Procedure Time intraoperative No
See also
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