Comparison of Interrupted Suturing Versus Continuous Suturing in Laparotomy Wound Closed.
Comparison of Outcome of Emergency Laparotomy Wound Closed by Interrupted Suturing Versus Continuous Suturing.
1 other identifier
interventional
184
1 country
1
Brief Summary
Emergency laparotomy is associated with high morbidity, particularly due to wound dehiscence and infection. Choosing an optimal suturing technique can significantly impact patient outcomes, but data on the comparison of interrupted suturing with continuous suturing in emergency settings is limited. Therefore, the current study was planned, aiming to compare the outcome of emergency laparotomy wounds closed by interrupted suturing versus continuous suturing.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Aug 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 14, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 14, 2026
CompletedFirst Submitted
Initial submission to the registry
May 15, 2026
CompletedFirst Posted
Study publicly available on registry
May 22, 2026
CompletedMay 22, 2026
May 1, 2026
6 months
May 15, 2026
May 15, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Wound dehiscence
The frequency of patients who experienced spontaneous opening of the midline laparotomy sutures within 10 days of surgery was noted.
10 days
Wound infection
The frequency of patients who showed the presence of pus or any discharge at the surgical wound site, which was accompanied by pain, fever, raised white blood cell count (\> 11000), swelling, and erythema, was noted.
10 days
Study Arms (2)
Group-A
EXPERIMENTALPatients went through interrupted closure with Smead Jones technique using prolene 1.
Group-B
EXPERIMENTALPatients went through continuous closure with prolene 1.
Interventions
Patients went through interrupted closure with Smead Jones technique using prolene 1.
Eligibility Criteria
You may qualify if:
- Patients of either gender
- Aged 18-60 years
- Undergoing emergency laparotomy
You may not qualify if:
- Unfit for surgery
- History of diabetes
- Immuno-compromised
- Pregnant/lactating mothers
- Malignancy
- Very low or very high body mass index (\< 15kg/m2 or \> 30kg/m2)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Benazir Bhutto Hospital/Rawalpindi Medical University and Allied Hospitals
Rawalpindi, Punjab Province, 46000, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Farhan Ahmed
Benazir Bhutto Hospital/Rawalpindi Medical University and Allied Hospitals, Rawalpindi
- STUDY DIRECTOR
Usman Qureshi, FCPS
Holy Family Hospital/Rawalpindi Medical University and Allied Hospitals, Rawalpindi
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Research Consultant
Study Record Dates
First Submitted
May 15, 2026
First Posted
May 22, 2026
Study Start
August 15, 2025
Primary Completion
February 14, 2026
Study Completion
February 14, 2026
Last Updated
May 22, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share
Data can be shared on a reasonable request.