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Clinical Trials/NCT06745505
NCT06745505CompletedNot Applicable

EFFECTIVENESS of PRE-OPERATIVE BOWEL PREPARATION VS NO BOWEL PREPARATION on OUTCOMES of PEDIATRIC COLORECTAL SURGERIES

Shaheed Zulfiqar Ali Bhutto Medical University1 site in 1 country62 target enrollmentStarted: July 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
62
Locations
1
Primary Endpoint
No difference in surgical outcome after bowel preparation

Study Overview

Brief Summary

To compare the effectiveness of pre-operative bowel preparation vs no bowel preparation on outcomes of pediatric colorectal surgeries.

Detailed Description

Objective was to compare the effectiveness of pre-operative bowel preparation vs no bowel preparation on outcomes of pediatric colorectal surgeries. After approval from the ethical committee, 62 patients fulfilling the inclusion criteria were enrolled in this study from outpatient department. All participants were examined physically in person by the primary investigator. After which the patients were divided randomly into two groups A and B, 31 patients in each group. Group A patients were undergone bowel preparation while group B patients were not undergone bowel preparation. All patients were operated by a single consultant pediatric surgeon with more than 10 years of experience. Patients were called for follow up weekly till 6 weeks. Hospital stay was noted at the time of discharge. Wound infection rate was assessed till 30th post-operative day while anastomotic leak was ruled out on clinical and radiologic exam if symptoms were present. All the data of this study were analyzed in SPSS version 26. We concluded that that there is no significant difference in surgical outcomes between the group receiving the bowel preparation versus the group not receiving the bowel preparation in terms of surgical site infection rate, anastomotic leak and length of hospital stay.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Diagnostic
Masking
Single (Participant)

Eligibility Criteria

Ages
6 Months to 12 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients with congenital condition such as Hirschsprung disease, anorectal malformation requiring pull through with or without covering colostomy.
  • •Patients with anorectal malformation requiring anorectoplasty with or without covering colostomy.
  • •Ileostomy/colostomy acquired due to intestinal perforation, intestinal obstruction, and trauma admitted for reversal.
  • •Age up to 12 years.
  • •Patients of both genders.

Exclusion Criteria

  • •Any associated congenital morbid anomaly having Meningomyelocoele, Muscular dystrophy (were assessed on clinical examination)
  • •Patients with behavior disorders such as autism (were assessed during psychiatric history and clinical examination)
  • •Patients with behavioral disorder are difficult to counsel and follow up

Arms & Interventions

Recieved Bowel Preparation

Experimental

Intervention: Bowel Preparation (Procedure)

Did not receive Bowel Preparation

Active Comparator

Intervention: Bowel Preparation (Procedure)

Outcomes

Primary Outcomes

No difference in surgical outcome after bowel preparation

Time Frame: 1 year

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mansoor Ahmed

Resident Pediatric Surgery

Shaheed Zulfiqar Ali Bhutto Medical University

Study Sites (1)

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