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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01739478
Acronym
PPAC
Enrollment
300
Registered
2012-12-03
Start date
Unknown
Completion date
2015-12-31
Last updated
2012-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Perianal Abscess

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.

Interventions

OTHERPacking of abscess cavity

Application of external dressing whilst abscess cavity heals

Sponsors

North Western Research Collaborative
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Time to wound healing in days, defined as complete epithelialisation of the abscess cavity.1 day to 6 weekstime to healing will be assessed in days

Secondary

MeasureTime frameDescription
Quality of life scores as determined by the Euro QoL EQ-5D-3L10 to 14 daysQuality 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

Other

MeasureTime frame
Abscess recurrence rate0 days to 12 months
Fistula-in-ano formation rate0 days to 18 months
Cost0 days to 18 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026