Primary Anastomosis Versus Enterostomy in the Surgical Treatment of Necrotising Enterocolitis
Primary Purpose
Necrotizing Enterocolitis
Status
Recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Primary anastomosis
Enterostomy
Sponsored by
About this trial
This is an interventional treatment trial for Necrotizing Enterocolitis focused on measuring Necrotizing Enterocolitis, Neonatal surgery, Primary anastomosis, Enterostomy
Eligibility Criteria
Inclusion Criteria:
- All neonates with confirmed NEC and require surgical intervention will be included
Exclusion Criteria:
- Neonates found to have NEC totalis and deemed unsalvageable;
- Neonates found to have multiple sites of gangrenous bowels which require more than two anastomoses;
- Neonates found to be extremely unstable cardiovascularly intra-operatively and can only withstand excision of gangrenous bowels, but will not allow anastomosis or stoma creation;
- Parents who do not agree to participate in the study
- Neonates found to have pathology other than NEC after recruitment (either on intraoperative findings or pathological findings on surgical specimens).
Sites / Locations
- Department of Surgery, University of Hong KongRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Primary anastomosis group
Enterostomy group
Arm Description
Outcomes
Primary Outcome Measures
Re-operation rate of the two surgical approaches
Secondary Outcome Measures
Wound-related problems
Wound problems not requiring re-operations e.g. wound infection; stomal prolapse; incisional hernia
Time to full enteral feeding
Time needed (in term of days) to achieve full enteral feeding (defined as 150ml/kg/day) and stoppage of parenteral feeding
Full Information
NCT ID
NCT04912453
First Posted
May 28, 2021
Last Updated
November 1, 2022
Sponsor
The University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT04912453
Brief Title
Primary Anastomosis Versus Enterostomy in the Surgical Treatment of Necrotising Enterocolitis
Official Title
A Randomised Controlled Trial to Compare Primary Anastomosis Versus Enterostomy in the Surgical Treatment of Necrotising Enterocolitis
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2021 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
January 31, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Hong Kong
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Necrotizing enterocolitis (NEC) is a devastating disease that affects the intestine of premature infants and is the most common surgical emergency in newborns. It is estimated that up to 10% of premature babies can suffer from this condition. Despite aggressive medical treatment, surgical intervention is necessary in up half of the cases for bowel necrosis or perforation and these often represent the more severe form of the disease. The advances in neonatal intensive care and surgical knowledge have resulted in improved survival rate in recent years.
For NEC patients with severe disease (i.e.) those with intestinal perforation or gangrenous bowel not responding to medical therapy, surgery with resection of diseased segments is the treatment of choice. Traditional surgical approach would be to resect the diseased bowel segment with formation of enterostomy. However, in a few advanced centres, primary anastomosis after the resection of diseased bowel segment is practised. Retrospective reports of the primary anastomosis approach have shown that this is also a viable option with no increased rate of peri-operative morbidity. It also has the advantage of avoiding a second operation for enterostomy closure. Nonetheless, prospective studies comparing the two approaches are lacking.
The proposed study will fill up the following knowledge gap on what the best surgical option for NEC at laparotomy is. The findings will help guide our practice for NEC patients in the future in order to provide them with the best possible and evidence-based care.
In this study, the investigators hypothesize that neonates with major NEC undergoing primary anastomosis after surgical resection is not inferior to neonates who have enterostomy, in terms of peri-operative morbidities.
Aim of the study is to compare the short term and medium term outcomes of NEC patients requiring surgical intervention who either receive primary anastomosis or enterostomy creation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Necrotizing Enterocolitis
Keywords
Necrotizing Enterocolitis, Neonatal surgery, Primary anastomosis, Enterostomy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
All neonates with confirmed NEC and require surgical intervention will be included. This is a local multi-centre study and neonates from the three centres which perform neonatal surgery will participate. At laparotomy, the diseased segment of intestine will be resected and the patients will then receive either primary anastomosis or enterostomy according to randomisation done pre-operatively.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Primary anastomosis group
Arm Type
Experimental
Arm Title
Enterostomy group
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Primary anastomosis
Intervention Description
At laparotomy, the diseased segment of intestine will be resected and the patients will then receive primary anastomosis
Intervention Type
Procedure
Intervention Name(s)
Enterostomy
Intervention Description
At laparotomy, the diseased segment of intestine will be resected and the patients will then receive enterostomy
Primary Outcome Measure Information:
Title
Re-operation rate of the two surgical approaches
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Wound-related problems
Description
Wound problems not requiring re-operations e.g. wound infection; stomal prolapse; incisional hernia
Time Frame
6 months
Title
Time to full enteral feeding
Description
Time needed (in term of days) to achieve full enteral feeding (defined as 150ml/kg/day) and stoppage of parenteral feeding
Time Frame
6 months
10. Eligibility
Sex
All
Maximum Age & Unit of Time
30 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All neonates with confirmed NEC and require surgical intervention will be included
Exclusion Criteria:
Neonates found to have NEC totalis and deemed unsalvageable;
Neonates found to have multiple sites of gangrenous bowels which require more than two anastomoses;
Neonates found to be extremely unstable cardiovascularly intra-operatively and can only withstand excision of gangrenous bowels, but will not allow anastomosis or stoma creation;
Parents who do not agree to participate in the study
Neonates found to have pathology other than NEC after recruitment (either on intraoperative findings or pathological findings on surgical specimens).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Adrian Fung, MBBS
Phone
+85222554850
Email
fungchiheng@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kenneth KY Wong, MD, PhD
Organizational Affiliation
The University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Surgery, University of Hong Kong
City
Hong Kong
ZIP/Postal Code
0000
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Adrian Fung, MBBS
Phone
+85222554850
Email
fungchiheng@gmail.com
12. IPD Sharing Statement
Learn more about this trial
Primary Anastomosis Versus Enterostomy in the Surgical Treatment of Necrotising Enterocolitis
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