Skip to content

comparison of surgical site infection rate in abdominal wounds using two different closure techniques

Primary skin closure versus delayed primary skin closure in reducing Surgical Site Infection in dirty midline abdominal operative wounds - A randomized controlled trialÂ

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/02/006685
Enrollment
66
Registered
2016-02-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- All patients operated for abdominal conditions in which the midline incision of the surgical wound falls into class 4 dirty abdominal wound according to the CDC classification

Interventions

Intervention1: Delayed primary closure: -consent obtained and randomly allocated into this group. -fascial closure with 1-0 prolene. -no subcutaneous sutures. -skin left open, packed with a sterile sa

Sponsors

JIPMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients operated for abdominal conditions in general surgery in which surgical incision falls into class-IV- dirty abdominal wound according to CDC which includes -Operative wound with acute purulent bacterial inflammation or perforated viscus -Operative wound where clean tissue is transected to gain access to a collection of pus -Fecal contamination -Retained devitalized tissue -Traumatic wound with delayed treatment ( after 4 hours) -Traumatic wound from dirty source/ Operative wound dirty -Retained foreign body

Exclusion criteria

Exclusion criteria: -Patientâ??s refusal -Patient treated outside before coming to the hospital -Patients requires re-exploration in the same hospital admission -Patients in whom primary rectus closure is not possible or in whom laparostoma is warranted -patient expires before discharge -patient less than 18 years of age

Design outcomes

Primary

MeasureTime frame
-Incidence of surgical site infection and degree of SSI (superficial incisional/ deep incisional) as per the definition of CDC in each group .Timepoint: -during hospital stay -at discharge -at first visit

Secondary

MeasureTime frame
-Length of hospital stay in days -Postoperative pain: third and fifth postoperative day -Patient satisfaction at the time of discharge from the hospital and at the first visit and after one month following discharge -Cosmetic outcome and scar appearance of the woundTimepoint: -at third and fifth post operative days -at discharge -at first visit -at one month following discharge

Countries

India

Contacts

Public ContactSuresh Kumar

JIPMER

drsureshkumar08@yahoo.com9788637893

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026