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CompletedNCT04832529Updated Aug 26, 2022

A Perianal Abscess Cavity Packing vs no Packing.

An interventional study of No packing of perianal abscess cavity in Perianal Abscess and Ischiorectal Abscess, sponsored by Dow University of Health Sciences. Completed at 1 site in Pakistan. Open to participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-08-26.

Sponsored by Dow University of Health Sciences · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year after the study started (first participant enrolled Mar 2020, registered Mar 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

This prospective randomized trial will be conducted in all patients undergoing packing or no packing for perianal abscess cavity after incision and drainage, for 6 months after approval from IRB in Surgical unit III, Civil Hospital Karachi. Patient will be selected simple random sampling technique based on inclusion criteria. Patient will be assessed for post-operative pain, healing of cavity and recurrence of abscess. At first time of debridement pus or tissue will be sent for culture and sensitivity, meanwhile broad-spectrum antibiotic will be started.

Questionnaire will be filled by PI for post-operative pain, recurrence of abscess, quality of life, wound healing, post operative fistula in ano and chronic post surgical pain either due to packing or no packing.

Read the detailed description

This is an experimental randomized control trial will start 6 months after approval from Institution Review Board. All patients with perianal abscess after incision and drainage cavity will be either packed or not after informed consent. Pack will be changed daily as regular dressing till healing occurs. Packing reduces bleeding and heals cavity by effect of dressing solution in which gauze is soaked. Other group with dressing will be changed daily and will be assessed for healing week. There is no pain in simple dressing applied over cavity. Patient will receive broad spectrum antibiotics according to pus or tissue culture. During this period, laboratory investigation CBC, CRP will be sent to check the response. Sits bath will be advised to both groups. Post-operative pain, cavity healing will be assessed by faculty.

02

Conditions studied

  • Perianal Abscess
  • Ischiorectal Abscess

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03

In context

Abscess

152 studies on the registry are indexed under Abscess; 22 are open to participants now.

This study's enrollment of 70 is below the median of 110 across 120 interventional studies indexed under Abscess.

Browse Abscess studies →

Lead sponsor

Dow University of Health Sciences is the lead sponsor of 179 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age greater than 18 years
  • Age less than 70 years
  • Perianal abscess

Exclusion criteria

Exclusion Criteria:

  • Suspected inflammatory bowel disease
  • Fournier's gangrene
  • Horseshoe/bilateral abscess
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
70 participants (actual)

Study arms

  • Active comparator
    Perianal abscess cavity packing

    Procedure: No packing of perianal abscess cavity

  • Experimental
    Perianal abscess cavity no packing

    Procedure: No packing of perianal abscess cavity

Interventions

  • ProcedureNo packing of perianal abscess cavity

    introducing new method to no packing of abscess cavity.

06

What researchers measure

Primary outcomes

  1. Post-operative pain

    Pain will be assessed via visual analogue scale from 1-10 while changing of dressing.

    Time frame: 14 days

Secondary outcomes

  1. Decreases hospital visit

    Hospital visits will be decreased when dressing only dressing to be done, not wound packing.

    Time frame: 3 weeks

07

Study locations

1 site
  • Dr Ruth K.M Pfau Civil Hospital
    Karachi, Sindh 75000, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 26, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04832529
Responsible party
Lajpat Rai (Principal Investigator, Dow University of Health Sciences) — Principal investigator
First posted
Apr 5, 2021
Start date
Mar 1, 2020
Primary completion
Jul 31, 2021
Completion
Jul 31, 2021
Last update
Aug 26, 2022

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2022. You cannot join it, but the record below documents what was studied.

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