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Not yet recruitingNCT07605403Updated May 26, 2026

Comparison of Outcome of Purse-string Versus Conventional Linear Wound Closure Techniques in Patients Undergoing Stoma Reversal

An interventional study of Purse-string wound closure and Conventional linear wound closure in Stoma Reversal Procedure, sponsored by Children Hospital Faisalabad. Not yet recruiting at 1 site in Pakistan. Open to participants aged 8 Months to 12 Years. Per ClinicalTrials.gov, last updated 2026-05-26.

Sponsored by Children Hospital Faisalabad · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jul 2026, 3 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
108
Allocation
Randomized
Ages
8 Months to 12 Years
Sex
All
01

Study summary

To compare outcomes of purse-string skin closure and conventional linear skin closure techniques in patients undergoing stoma reversal

Read the detailed description

Upon receiving permission from the ERC, children who fulfill the operational definitions and inclusion criteria will be enrolled in the research after informed consent. Children of both genders, age 8 months to 12 years, undergoing ileostomy or colostomy reversal will be included. All patients will be divided into two groups by lottery method by offering them to pick up slip. In group A patients, skin wound closure after stoma reversal will be done with technique of purse-string closure. In group B patients, skin closure after reversal will be done with technique of conventional linear closure. All procedures will be performed by the same. Outcome of surgery will be noted in every patient of both groups as per operational definition. This all data will be recorded on a specially designed proforma

02

Conditions studied

  • Stoma Reversal Procedure
03

In context

Lead sponsor

Children Hospital Faisalabad is the lead sponsor of 5 studies on the registry; 4 are open to participants now.

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

04

Who can participate

Ages eligible
8 Months to 12 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Children of both genders
  • 8 months to 12 years
  • Undergoing ileostomy or colostomy reversal will be include

Exclusion criteria

Exclusion Criteria:

    • Patients with Re-current stoma prolapse

      • Patients with Re-do stomas
      • Patients with underlying chronic inflammatory and neoplastic conditions (Tuberculosis, Maligency
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
108 participants (estimated)

Study arms

  • Experimental
    Purse-string closure group

    Patients undergoing stoma reversal in whom wound closure will be performed using the purse-string closure technique.

    Procedure: Purse-string wound closure

  • Active comparator
    Conventional linear closure group

    Patients undergoing stoma reversal in whom wound closure will be performed using the conventional linear closure technique

    Procedure: Conventional linear wound closure

Interventions

  • ProcedurePurse-string wound closure

    Closure of stoma reversal wound using purse-string approximation technique

  • ProcedureConventional linear wound closure

    Closure of stoma reversal wound using conventional linear skin closure technique.

06

What researchers measure

Primary outcomes

  1. Surgical Site Infections

    The presence of infection at the wound site, identified by clinical signs (e.g., redness, swelling, pus)

    Time frame: 7 days

  2. Time for wound healing

    The duration from the surgical procedure until the wound is fully healed. It will be assessed on clinical examination of wound closure, including inspection for signs of epithelialization and the absence of gaps or dehiscence.

    Time frame: 6 weeks

  3. Length of stay

    The total number of days a patient in a hospital from admission till discharge date.

    Time frame: 10 days

07

Study locations

1 site
  • Children hospital Faisalabad
    Faisalābad, Punjab Province 38000, Pakistan
08

References and documents

Individual participant data

Plan to share: Undecided

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 May 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07605403
Lead sponsor
Children Hospital Faisalabad
Responsible party
Dr. Sayed Elyas (Principal investigator department of Pediatric Surgery, Children Hospital Faisalabad) — Principal investigator
First posted
May 26, 2026
Start date
Jun 15, 2026 (estimated)
Primary completion
Jul 2026 (estimated)
Completion
Jul 2026 (estimated)
Last update
May 26, 2026

Study contacts

Sayed Elyas
Contact
elyas.sadat100@gmail.com
+923194440578

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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