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Clinical Trials/NCT05943223
NCT05943223CompletedPhase 2

Assessing the Longitudinal Outcomes of Piperacillin/Tazobactam Versus ceftriAxone and Metronidazole for Children With Perforated Appendicitis (ALPACA): a Randomized Controlled Trial

McMaster Children's Hospital1 site in 1 country16 target enrollmentStarted: September 9, 2024Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 2
Status
Completed
Enrollment
16
Locations
1
Primary Endpoint
Length of stay

Study Overview

Brief Summary

This study is an internal pilot for a multicenter, blinded randomized controlled trial. The purpose of the multicenter trial is to determine whether post-operative piperacillin/tazobactam is more effective than ceftriaxone and metronidazole for children treated with laparoscopic appendectomy for perforated appendicitis. We plan to conduct an internal pilot study to determine whether a blinded multicenter randomized controlled trial is feasible.

Detailed Description

Acute appendicitis is the most common indication for emergency surgery in children. The management of this condition is typically an urgent laparoscopic appendectomy under general anesthesia. If the appendix is found to be perforated at the time of surgery, then patients need to stay in hospital for intravenous antibiotics. Patients who do not respond to antibiotic therapy experience prolonged length of stay, need for additional procedures (such as percutaneous drain insertion), or other complications. This represents significant morbidity for patients and their families.

Children with perforated appendicitis were previously treated with post-operative ampicillin, gentamicin, and metronidazole (also known as "triple therapy"). In 2008, a randomized controlled trial showed that triple therapy is non-inferior to ceftriaxone and metronidazole (CM) in terms of intra-abdominal abscess formation and wound infection. CM is also less expensive and has a simplified dosing regimen. As such, post-operative CM became the standard of care for perforated appendicitis at most children's hospitals.

In 2021, an open-label RCT suggested that piperacillin/tazobactam (PT) is more effective than CM for children with perforated appendicitis. Patients randomized to PT had a reduced rate of intra-abdominal abscess formation compared to those treated with CM (odds ratio (OR) 4.80, p=0.002). This trial was not blinded and there was no allocation concealment. In contrast, a multicenter, observational study reported no difference in the rate of intra-abdominal abscess formation among patients treated with PT compared to CM. The conflicting results of these two studies add further uncertainty regarding the choice of antibiotics for these patients.

Another factor that should be considered regarding the use of PT versus CM in children with perforated appendicitis is antibiotic stewardship. PT is a broad-spectrum antibiotic with increased effectiveness against Pseudomonas aeruginosa and resistant Escherichia coli. As a result, this medication is often reserved for patients with confirmed Pseudomonas infection, oncology patients with febrile neutropenia, or those who are critically ill and admitted to the intensive care unit.

The current study is an internal pilot for a multicenter, blinded randomized controlled trial. The purpose of the multicenter trial is to determine whether post-operative piperacillin/tazobactam is more effective than ceftriaxone and metronidazole for children treated with laparoscopic appendectomy for perforated appendicitis. We plan to conduct an internal pilot study to determine whether a blinded multicenter randomized controlled trial is feasible.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
— to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Laparoscopic appendectomy
  • Perforated appendicitis confirmed intra-operatively (i.e., visible hole in appendix, fecalith found in peritoneal cavity, intra-abdominal abscess, and/or purulent fluid in peritoneal cavity)

Exclusion Criteria

  • Non-operative treatment (e.g., due to abscess)
  • Interval laparoscopic appendectomy
  • Conversion to open procedure
  • Non-perforated appendicitis
  • Confirmed or suspected allergy to penicillins or cephalosporins
  • Renal impairment

Arms & Interventions

Ceftriaxone and metronidazole

Active Comparator

Intervention: CefTRIAXone Injection (Drug)

Piperacillin/tazobactam

Experimental

Intervention: Normal saline (Drug)

Ceftriaxone and metronidazole

Active Comparator

Intervention: Metronidazole Injection (Drug)

Piperacillin/tazobactam

Experimental

Intervention: Piperacillin/tazobactam (Drug)

Outcomes

Primary Outcomes

Length of stay

Time Frame: Index admission

Length of stay in hospital during index admission

Secondary Outcomes

  • Parenteral nutrition(Within 30 days of surgery)
  • Post-operative ultrasound(Within 30 days of surgery)
  • Clostridium difficile infection(Within 30 days of surgery)
  • Readmission to hospital(Within 30 days of surgery)
  • Exit survey(Telephone call 3 months after surgery)
  • Return to the emergency department(Within 30 days of surgery)
  • Deep or organ-space surgical site infection(Within 30 days of surgery)
  • Late complications(Telephone call 3 months after surgery)
  • Percutaneous drain insertion(Within 30 days of surgery)
  • Insertion of Peripherally Inserted Central Catheter (PICC)(Within 30 days of surgery)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Michael Livingston

Pediatric Surgeon

McMaster Children's Hospital

Study Sites (1)

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