ClinConnect ClinConnect Logo
Search / Trial NCT05289713

Appendectomy vs. Symptomatic Treatment in Uncomplicated Acute Appendicitis Among Pediatric Patients

Launched by HELSINKI UNIVERSITY CENTRAL HOSPITAL · Mar 11, 2022

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Uncomplicated Acute Appendicitis Symptomatic Treatment Spontaneous Resolution

ClinConnect Summary

The APPSYPP trial is a study that aims to compare two different treatments for children aged 7 to 15 who have been diagnosed with uncomplicated acute appendicitis, which is a condition where the appendix becomes inflamed but has not caused any serious complications. In this trial, some children will receive an emergency surgery called an appendectomy to remove the appendix, while others will receive symptomatic treatment, which means they will be given care to manage their symptoms without surgery. The goal is to see which approach is more effective in treating this condition.

To participate in this trial, children must be between 7 and 15 years old, have imaging tests like an ultrasound or MRI showing uncomplicated appendicitis, and have a certain level of a blood marker called CRP. Participants can expect to be closely monitored in a hospital setting, especially those receiving symptomatic treatment, which includes receiving fluids and pain relief for at least 24 hours. The study will track their recovery for 30 days to determine how well each treatment works and if there are any complications. This research is important as it may help doctors decide the best way to treat pediatric appendicitis in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • age 7-15 years
  • clinical diagnosis of uncomplicated acute appendicitis confirmed by US and/or MRI: adequately visualized appendix with a diameter of 6.1-11.0 mm without evidence of perforation, abscess, appendicolith or tumor suspicion
  • CRP ≤ 65 mg/l
  • Exclusion Criteria:
  • inability to give informed consent
  • age under 7 or over 15 years
  • antibiotic administration within 14 days prior to enrolment
  • any previous treatment for acute appendicitis
  • severe nausea and/or vomiting preventing oral fluid intake
  • systemic disease potentially compromising the safety of symptomatic treatment of acute appendicitis (e.g. type 2 diabetes, malignancy, immune deficiency, or a medical condition requiring immunosuppressant medication)
  • diffuse peritonitis or complicated acute appendicitis at imaging (perforation, abscess, appendicolith or tumor suspicion)
  • inadequately visualized appendix
  • age and sex adjusted BMI over 27 kg/m2 and no MRI performed
  • CRP \> 65 mg/l.

About Helsinki University Central Hospital

Helsinki University Central Hospital (HUCH) is a leading academic medical institution in Finland, dedicated to advancing healthcare through innovative research and clinical excellence. As a pivotal sponsor of clinical trials, HUCH integrates cutting-edge medical practices with rigorous scientific inquiry, fostering collaborations between researchers, healthcare professionals, and patients. The hospital is committed to enhancing patient outcomes and contributing to the global body of medical knowledge by conducting high-quality, ethically sound clinical studies across a diverse range of therapeutic areas. With a strong emphasis on education and training, HUCH plays a vital role in shaping the next generation of healthcare leaders and researchers.

Locations

Helsinki, , Finland

Patients applied

0 patients applied

Trial Officials

Janne Suominen, MD, PhD

Principal Investigator

Helsinki University Central Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials