NCT01186900
Terminated
Not Applicable
Comparison of Ultrasound-Guided Needle Aspiration and Open Incision and Drainage in the Management of Cutaneous Abscesses
ConditionsAbscess
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Abscess
- Sponsor
- Ottawa Hospital Research Institute
- Enrollment
- 20
- Locations
- 1
- Primary Endpoint
- Patient satisfaction
- Status
- Terminated
- Last Updated
- 14 years ago
Overview
Brief Summary
The investigators propose to conduct a, two armed, randomized, controlled pilot study to assess the clinical effects of a) open incision, drainage with daily packing changes, compared to b) Ultrasound guided needle aspiration, in drainage of uncomplicated cutaneous abscesses below the skin surface of adult emergency department patients using concealed allocation in evaluating patient satisfaction.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients presenting to the Civic Campus emergency department of The Ottawa Hospital with an abscess less than 5 cm diameter, as judged by the attending emergency physician (measurement with tape measure for diameter) between the hours of 7 am and 10 pm will be approached for possible enrollment. Ultrasound will be used to assess the appropriate exclusion criteria.
Exclusion Criteria
- •Patients under the age of 18 years,
- •Patients with a Glasgow coma scale score of \<15 (i.e. not completely alert and oriented),
- •Patients suspected of having necrotising fascitis,
- •Patients with hemodynamic instability (defined as SBP \<90, and/or HR \>110),
- •Patients admitted to hospital,
- •Patients who are neither French nor English speaking,
- •Patients who are not available for telephone follow-up (i.e. homeless).
- •Ultrasound image demonstrates that the abscess is not compressible (generally indicates that the contents of the cyst includes solids, which would not be amenable to aspiration)
- •Ultrasound demonstrates that there is no abscess to manage,
- •Patients with perianal abscesses who have either Crohn's disease or ulcerative colitis or known perirectal fistula,
Outcomes
Primary Outcomes
Patient satisfaction
Time Frame: 7 days
Secondary Outcomes
- Failure rate(7 days)
Study Sites (1)
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