McMaster Children's Hospital
Hamilton, Ontario, L8N 3Z5, Canada
NCT Number: NCT05943223
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.
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Notify MeUp to 18 year
All sexes
Interventional
Phase 2
Hamilton, Ontario, L8N 3Z5, Canada
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Post-operative piperacillin/tazobactam 100 mg/kg IV q8h (to a maximum of 4.5 g IV q8h)
Post-operative normal saline 50 mL once daily
Post-operative ceftriaxone 50 mg/kg IV once daily (to a maximum of 2 g IV once daily)
Post-operative metronidazole 10 mg/kg IV q8h (to a maximum of 500 mg IV q8h)
Time frame: Index admission
Length of stay in hospital during index admission
Time frame: Within 30 days of surgery
Percutaneous drain insertion by Interventional Radiology
Time frame: Within 30 days of surgery
Deep or organ-space surgical site infection
Time frame: Within 30 days of surgery
Insertion of Peripherally Inserted Central Catheter (PICC)
Time frame: Within 30 days of surgery
Need for parenteral nutrition
Time frame: Within 30 days of surgery
Need for post-operative ultrasound
Time frame: Within 30 days of surgery
Clostridium difficile infection (confirmed with stool sample and requiring treatment)
Time frame: Within 30 days of surgery
Return to the emergency department within 30 days of surgery
Time frame: Within 30 days of surgery
Readmission to hospital within 30 days of surgery
Time frame: Telephone call 3 months after surgery
Telephone confirmation of no additional complications related to perforated appendicitis requiring assessment in clinic, emergency department visit, or admission to hospital
Time frame: Telephone call 3 months after surgery
Parents will complete a descriptive questionnaire about the study by telephone
Time frame: Through study completion (average of 1 year)
Number of participants randomized per month
Time frame: Through study completion (average of 1 year)
Number of participants who consent to participate divided by those who are approached for consent
Time frame: Through study completion (average of 1 year)
Number of participants who do not receive study treatments within 8 hours of surgery, miss a scheduled study treatment, and/or experience treatment crossover divided by those randomized
Time frame: Through study completion (average of 1 year)
Number of participants who cannot be contacted by phone 3 months after discharge from hospital divided by those randomized
Time frame: Through study completion (average of 1 year)
Total cost of internal pilot study in Canadian dollars divided by the number of participants randomized
McMaster Children's Hospital
Other
Assessing the Longitudinal Outcomes of Piperacillin/Tazobactam Versus ceftriAxone and Metronidazole for Children With Perforated Appendicitis (ALPACA): a Randomized Controlled Trial
Acronym: ALPACA
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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