Role of Intravenous Versus Home Oral Antibiotics in Perforated Appendicitis
Primary Purpose
Perforated Appendicitis
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
home intravenous ertapenem
home oral amoxicillin-clavulanate
peripheral inserted central Catheter
Sponsored by
About this trial
This is an interventional treatment trial for Perforated Appendicitis focused on measuring appendectomy
Eligibility Criteria
Inclusion Criteria:
- Patients 4-17 years of age with perforated acute appendicitis diagnosed at time of appendectomy.
Exclusion Criteria:
- Patients with a known severe allergy to penicillin (anaphylaxis), prior severe side effects from ertapenem or amoxicillin-clavulanate, pregnancy, or previous drainage procedure for abscess and/or fluid collection related to appendicitis.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
home intravenous ertapenem and PICC
home oral amoxicillin-clavulanate
Arm Description
Placement of peripheral inserted central catheter (PICC) and completion of ten day antibiotic treatment with home (IV) ertapenem (Drug Class:carbapenem antibiotic) (15 mg/kg IV every twelve hours not to exceed 1 gm/day for ages <13; age 13 or greater, then 1 gm daily)
Completion of ten day antibiotic treatment with home oral amoxicillin-clavulanate(Drug Class:beta lactam antibiotic)(15mg/kg every eight hours or 22.5mg/kg extended release tablets every twelve hours).
Outcomes
Primary Outcome Measures
Number of Participants With Postoperative Abscess
Number of Postoperative Abscess, thirty-day postoperative
Number of Participants With Wound Infections
Number of Wound Infections, 30-days postoperative
Number Participants With Readmission Within 30 Days
Number of Readmission within 30 days postoperative
Hospital Charge
Cost of Hospital services
Secondary Outcome Measures
Full Information
NCT ID
NCT02724410
First Posted
March 15, 2016
Last Updated
April 20, 2022
Sponsor
Wake Forest University Health Sciences
1. Study Identification
Unique Protocol Identification Number
NCT02724410
Brief Title
Role of Intravenous Versus Home Oral Antibiotics in Perforated Appendicitis
Official Title
Home Intravenous Versus Oral Antibiotics Following Appendectomy for Perforated Appendicitis in Children, a Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
November 2013 (Actual)
Study Completion Date
November 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To compare the effect of a single-agent home intravenous (IV) versus oral antibiotic therapy on complication rates and resource utilization following appendectomy for perforated appendicitis
Detailed Description
Appendicitis is the most common cause of abdominal pain requiring emergent surgical intervention in children and approximately one third of patients present with perforation. Perforated appendicitis has been demonstrated to have a significant impact on patients and families due to the prolonged hospitalization, high complication rates, and tremendous economic burden from treatment. The most significant complication following operative treatment of perforated appendicitis is intra-abdominal abscess, which develops in approximately 20% of children following appendectomy in recent literature. Due to this frequent and morbid complication, continued research has been driven at determining the most efficacious and cost-effective postoperative antibiotic treatment regimen to reduce post-operative abscess. As postoperative abscess rates following appendectomy for perforated appendicitis remain high, the primary aim of this study was to evaluate a new postoperative antibiotic treatment regimen based on single daily dosing ertapenem while inpatient with randomization into ten day completion course of home antibiotics with IV ertapenem versus oral amoxicillin/clavulanate. The hypothesis is that the ertapenem based regimen will offer reduced rates of postoperative abscess, with no major difference between completion courses of home IV versus oral antibiotics.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Perforated Appendicitis
Keywords
appendectomy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
82 (Actual)
8. Arms, Groups, and Interventions
Arm Title
home intravenous ertapenem and PICC
Arm Type
Active Comparator
Arm Description
Placement of peripheral inserted central catheter (PICC) and completion of ten day antibiotic treatment with home (IV) ertapenem (Drug Class:carbapenem antibiotic) (15 mg/kg IV every twelve hours not to exceed 1 gm/day for ages <13; age 13 or greater, then 1 gm daily)
Arm Title
home oral amoxicillin-clavulanate
Arm Type
Experimental
Arm Description
Completion of ten day antibiotic treatment with home oral amoxicillin-clavulanate(Drug Class:beta lactam antibiotic)(15mg/kg every eight hours or 22.5mg/kg extended release tablets every twelve hours).
Intervention Type
Drug
Intervention Name(s)
home intravenous ertapenem
Other Intervention Name(s)
Invanz
Intervention Description
see arm description
Intervention Type
Drug
Intervention Name(s)
home oral amoxicillin-clavulanate
Other Intervention Name(s)
Augmentin
Intervention Description
see arm description
Intervention Type
Device
Intervention Name(s)
peripheral inserted central Catheter
Other Intervention Name(s)
PICC
Intervention Description
All patients undergoing home intravenous ertapenem will require placement of peripheral inserted central Catheter (PICC) for home delivery of antibiotics.
Primary Outcome Measure Information:
Title
Number of Participants With Postoperative Abscess
Description
Number of Postoperative Abscess, thirty-day postoperative
Time Frame
Thirty days after appendectomy
Title
Number of Participants With Wound Infections
Description
Number of Wound Infections, 30-days postoperative
Time Frame
Thirty days following appendectomy
Title
Number Participants With Readmission Within 30 Days
Description
Number of Readmission within 30 days postoperative
Time Frame
Thirty days following appendectomy
Title
Hospital Charge
Description
Cost of Hospital services
Time Frame
Thirty days following appendectomy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients 4-17 years of age with perforated acute appendicitis diagnosed at time of appendectomy.
Exclusion Criteria:
Patients with a known severe allergy to penicillin (anaphylaxis), prior severe side effects from ertapenem or amoxicillin-clavulanate, pregnancy, or previous drainage procedure for abscess and/or fluid collection related to appendicitis.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brant T Heniford, M.D.
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Role of Intravenous Versus Home Oral Antibiotics in Perforated Appendicitis
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