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Are Post-operative Antibiotics Indicated in Simple Appendicitis?

Primary Purpose

Appendicitis

Status
Unknown status
Phase
Not Applicable
Locations
Australia
Study Type
Interventional
Intervention
metronidazole and cephalzolin
Sponsored by
Monash University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Appendicitis focused on measuring Paediatric, Simple, Non-perforated

Eligibility Criteria

4 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients who have their appendix removed and are found on operation to have 'simple appendicitis' as defined in the Cochrane review[7]. That is an appendix that is non-inflamed, acutely inflamed, phlegmonous, suppurative or mildly inflamed.

Exclusion Criteria:

  • Patients who on operation are found to have 'complicated appendicitis' defined as an appendix that is gangrenous or perforated.
  • Patients who pre-operatively appear to be acutely septic or for another reason require extended antibiotic therapy.
  • Patients who, at operation, are found to have other pathology e.g. Meckel's Diverticulum, Intussusception; requiring surgical or medical intervention.
  • Any patient whose guardian does not wish for them to participate in the study.
  • Patients who have additional co-morbidities, including diabetes, immuno-suppression, cardiac, renal or liver failure.
  • If the child continues to show sign of sepsis, in terms of fever, tachycardia, he/she will be discontinued from the study and be given additional doses of antibiotics, as clinically indicated.

Sites / Locations

  • Monash Medical Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Single dose of antibiotics

Three doses of antibiotics

Arm Description

This group will receive one dose of IV metronidazole (12.5mg/kg up to 500mg) and cefazolin (25mg/kg up to 1g) in the pre-operative period and two post-operative IV 'doses' of normal saline 8 and 16 hours after the pre-operative dose, which will act as a placebo and facilitate blinding.

This group will receive one pre-operative dose of IV metronidazole (12.5mg/kg up to 500mg) and cefazolin (25mg/kg up to 1g) and two post-operative doses of IV metronidazole (12.5mg/kg up to 500mg) and cefazolin (25mg/kg up to 1g) 8 and 16 hours after the pre-operative dose.

Outcomes

Primary Outcome Measures

Presence of post-operative infection in the six weeks following appendectomy
Defined by wound infection, fever (>38.5) or evidence of sepsis.
Requirement of further antibiotic therapy in the six weeks following appendectomy
Administration of antibiotics either by hospital or general practitioner in the 6 week post-operative period.

Secondary Outcome Measures

Time to discharge taken from the time of operation to the time the child first satisfied the discharge criteria
Discharge criteria: Pain adequately controlled with oral analgesia Tolerating full diet Afebrile
Re-admission in the six weeks following appendectomy
Re-admission to the treating hospital or any other hospital in the 6 weeks post-operative period.

Full Information

First Posted
August 18, 2011
Last Updated
August 18, 2011
Sponsor
Monash University
Collaborators
Monash Medical Centre
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1. Study Identification

Unique Protocol Identification Number
NCT01420367
Brief Title
Are Post-operative Antibiotics Indicated in Simple Appendicitis?
Official Title
Are Post-operative Antibiotics Indicated in Simple Appendicitis? A Prospective Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2011
Overall Recruitment Status
Unknown status
Study Start Date
November 2011 (undefined)
Primary Completion Date
November 2013 (Anticipated)
Study Completion Date
December 2013 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Monash University
Collaborators
Monash Medical Centre

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Hypothesis: A single dose of prophylactic antibiotics is as effective as a three dose regime in preventing post-operative complications in paediatric patients with simple appendicitis. This project will compare patients 16 years and under with simple appendicitis (appendicitis that is not perforated or gangrenous). Patients will be randomly divided into two groups; Group one will receive a single pre-operative dose of antibiotics (metronidazole 12.5mg/kg up to 500mg and cefazolin 25mg/kg up to 1g) and two 'doses' of normal saline (placebo) eight and sixteen hours after the initial dose, respectively. Group two will receive one pre-operative dose of antibiotics (metronidazole 12.5mg/kg up to 500mg and cefazolin 25mg/kg up to 1g) and two post-operative doses, eight and sixteen hours after the first dose, respectively. Group allocation will be concealed from the patient and their guardian, the treating surgical team and outcome assessors (triple blinded). A process to rapidly reveal group allocation if required will be in place. The aim of the study is to determine if a single dose of antibiotics is as effective as three doses in preventing post-operative infection. This will be assessed by comparing: Duration of hospital stay from operation until discharge, based on a standardised discharge criteria. Development of wound infection or requirement of antibiotics in the six weeks post-operation Need for re-admission. Information will be collected prospectively from each patient's hospital notes and from a follow-up phone call six weeks after the operation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Appendicitis
Keywords
Paediatric, Simple, Non-perforated

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Single dose of antibiotics
Arm Type
Experimental
Arm Description
This group will receive one dose of IV metronidazole (12.5mg/kg up to 500mg) and cefazolin (25mg/kg up to 1g) in the pre-operative period and two post-operative IV 'doses' of normal saline 8 and 16 hours after the pre-operative dose, which will act as a placebo and facilitate blinding.
Arm Title
Three doses of antibiotics
Arm Type
Active Comparator
Arm Description
This group will receive one pre-operative dose of IV metronidazole (12.5mg/kg up to 500mg) and cefazolin (25mg/kg up to 1g) and two post-operative doses of IV metronidazole (12.5mg/kg up to 500mg) and cefazolin (25mg/kg up to 1g) 8 and 16 hours after the pre-operative dose.
Intervention Type
Drug
Intervention Name(s)
metronidazole and cephalzolin
Intervention Description
IV doses of metronidazole (12.5mg/kg up to 500mg) and cefazolin (25mg/kg up to 1g). One dose for study arm, two for comparative arm.
Primary Outcome Measure Information:
Title
Presence of post-operative infection in the six weeks following appendectomy
Description
Defined by wound infection, fever (>38.5) or evidence of sepsis.
Time Frame
6 weeks
Title
Requirement of further antibiotic therapy in the six weeks following appendectomy
Description
Administration of antibiotics either by hospital or general practitioner in the 6 week post-operative period.
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Time to discharge taken from the time of operation to the time the child first satisfied the discharge criteria
Description
Discharge criteria: Pain adequately controlled with oral analgesia Tolerating full diet Afebrile
Time Frame
1 week
Title
Re-admission in the six weeks following appendectomy
Description
Re-admission to the treating hospital or any other hospital in the 6 weeks post-operative period.
Time Frame
6 weeks

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: All patients who have their appendix removed and are found on operation to have 'simple appendicitis' as defined in the Cochrane review[7]. That is an appendix that is non-inflamed, acutely inflamed, phlegmonous, suppurative or mildly inflamed. Exclusion Criteria: Patients who on operation are found to have 'complicated appendicitis' defined as an appendix that is gangrenous or perforated. Patients who pre-operatively appear to be acutely septic or for another reason require extended antibiotic therapy. Patients who, at operation, are found to have other pathology e.g. Meckel's Diverticulum, Intussusception; requiring surgical or medical intervention. Any patient whose guardian does not wish for them to participate in the study. Patients who have additional co-morbidities, including diabetes, immuno-suppression, cardiac, renal or liver failure. If the child continues to show sign of sepsis, in terms of fever, tachycardia, he/she will be discontinued from the study and be given additional doses of antibiotics, as clinically indicated.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nicole Mennie, MBBS
Email
nmmen4@student.monash.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Wei Cheng, MBBS
Phone
+61395945500
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicole Mennie, MBBS
Organizational Affiliation
Monash University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wei Cheng, MBBS
Organizational Affiliation
Monash Medical Centre
Official's Role
Study Director
Facility Information:
Facility Name
Monash Medical Centre
City
Clayton
State/Province
Victoria
ZIP/Postal Code
3168
Country
Australia
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wei Cheng, MBBS
Phone
+61395945500
First Name & Middle Initial & Last Name & Degree
N Mennie, MBBS
Email
nmmen4@student.monash.edu
First Name & Middle Initial & Last Name & Degree
Nicole M Mennie, MBBS
First Name & Middle Initial & Last Name & Degree
Wei Cheng, MBBS
First Name & Middle Initial & Last Name & Degree
Peter Ferguson, MBBS

12. IPD Sharing Statement

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Are Post-operative Antibiotics Indicated in Simple Appendicitis?

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