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NCT Number: NCT05943223

Piperacillin/Tazobactam Versus ceftriAxone and Metronidazole for Children With Perforated Appendicitis (ALPACA)

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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Key information

Age range

Up to 18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

McMaster Children's Hospital

Hamilton, Ontario, L8N 3Z5, Canada

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Piperacillin/tazobactam

Drug

Post-operative piperacillin/tazobactam 100 mg/kg IV q8h (to a maximum of 4.5 g IV q8h)

normal saline

Drug

Post-operative normal saline 50 mL once daily

CefTRIAXone Injection

Drug

Post-operative ceftriaxone 50 mg/kg IV once daily (to a maximum of 2 g IV once daily)

Metronidazole Injection

Drug

Post-operative metronidazole 10 mg/kg IV q8h (to a maximum of 500 mg IV q8h)

Primary outcomes

  1. Length of stay

    Time frame: Index admission

    Length of stay in hospital during index admission

Secondary outcomes

  1. Percutaneous drain insertion

    Time frame: Within 30 days of surgery

    Percutaneous drain insertion by Interventional Radiology

  2. Deep or organ-space surgical site infection

    Time frame: Within 30 days of surgery

    Deep or organ-space surgical site infection

  3. Insertion of Peripherally Inserted Central Catheter (PICC)

    Time frame: Within 30 days of surgery

    Insertion of Peripherally Inserted Central Catheter (PICC)

  4. Parenteral nutrition

    Time frame: Within 30 days of surgery

    Need for parenteral nutrition

  5. Post-operative ultrasound

    Time frame: Within 30 days of surgery

    Need for post-operative ultrasound

  6. Clostridium difficile infection

    Time frame: Within 30 days of surgery

    Clostridium difficile infection (confirmed with stool sample and requiring treatment)

  7. Return to the emergency department

    Time frame: Within 30 days of surgery

    Return to the emergency department within 30 days of surgery

  8. Readmission to hospital

    Time frame: Within 30 days of surgery

    Readmission to hospital within 30 days of surgery

  9. Late complications

    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

  10. Exit survey

    Time frame: Telephone call 3 months after surgery

    Parents will complete a descriptive questionnaire about the study by telephone

Other outcomes

  1. Recruitment rate

    Time frame: Through study completion (average of 1 year)

    Number of participants randomized per month

  2. Consent rate

    Time frame: Through study completion (average of 1 year)

    Number of participants who consent to participate divided by those who are approached for consent

  3. Rate of protocol violations

    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

  4. Rate of loss to follow-up

    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

  5. Cost of trial

    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

Sponsors and collaborators

Lead sponsor

McMaster Children's Hospital

Other

Registry information

Official study title

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

Acronym: ALPACA

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jul 13, 2023
Registry last updated
Jul 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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