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Packing of Perianal Abscess Cavities Trial: A Randomised Multicentre Trial Comparing Packing With Non-packing of the Abscess Cavity

Not Applicable
Conditions
Perianal Abscess
Interventions
Other: Packing of abscess cavity
Other: External dressing
Registration Number
NCT01739478
Lead Sponsor
North Western Research Collaborative
Brief Summary

The aim of this study is to compare the effect of packing and non-packing on the healing rate of perianal abscess cavities. Secondary objectives are to assess quality of life, cost effectiveness and rate of abscess recurrence and fistula-in-ano formation. If there is no difference in time to healing and non-packing is shown to be safe, acceptable to the patient and cost effective, this approach may become more widely accepted.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
300
Inclusion Criteria
  • Clinical diagnosis of acute primary perianal abscess
  • Have undergone surgical incision and drainage as an emergency
Exclusion Criteria
  • The abscess is the sequelae of concurrent disease or trauma
  • Fourniers gangrene is suspected
  • Unable to give informed consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Packing of abscess cavityPacking of abscess cavityCurrent practice
Packing of abscess cavityExternal dressingCurrent practice
Non-packing of abscess cavityExternal dressing-
Primary Outcome Measures
NameTimeMethod
Time to wound healing in days, defined as complete epithelialisation of the abscess cavity.1 day to 6 weeks

time to healing will be assessed in days

Secondary Outcome Measures
NameTimeMethod
Quality of life scores as determined by the Euro QoL EQ-5D-3L10 to 14 days

Quality of life scores as determined by the Euro QoL EQ-5D-3L will be measured at 10-14 days following incision and drainage of abscess

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