Improving recovery for children after appendectomy using ERAS protocol
Effect of Enhanced Recovery After Surgery Protocol Based Care on Patient Outcomes in Children With Appendicitis: a Randomized Controlled Trial
This study is testing if a special recovery plan can help kids heal better and faster after having their appendix removed.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 68 (estimated) |
| Ages | 6 Years to 18 Years |
| Sex | All |
| Sponsor | Karadeniz Technical University Academic / other |
| Locations | 1 site (Trabzon) |
| Trial ID | NCT05962320 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of the Enhanced Recovery After Surgery (ERAS) protocol on clinical outcomes for pediatric patients undergoing appendectomy. It aims to implement a series of preoperative, intraoperative, and postoperative interventions designed to enhance recovery, reduce pain, and shorten hospital stays. The study will measure various outcomes, including postoperative pain levels, time to mobilization, and overall length of hospital stay, to assess the effectiveness of the ERAS protocol in this population.
Who should consider this trial
Good fit: Ideal candidates for this study are children aged 6 to 18 years who are scheduled to undergo an appendectomy.
Not a fit: Patients with significant comorbidities or contraindications that may hinder mobilization or oral feeding will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to faster recovery times and reduced hospital stays for children undergoing appendectomy.
How similar studies have performed: Previous studies utilizing the ERAS protocol in surgical settings have shown promising results in improving recovery outcomes, suggesting this approach is both tested and effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥6 years and ≤18 years, girls or boys * Underwent appendectomy * Written informed consent or requirements of local/national ethical committee Exclusion Criteria: * ASA (American Society of Anesthesiologists, ASA) score of ≥ 3 * Any comorbidity/contraindication that may prevent mobilization and oral feeding
Where this trial is running
Trabzon
- Karadeniz Technical University — Trabzon, Turkey (Recruiting)
Study contacts
- Principal investigator: Buket MERAL, Msc — Karadeniz Technical University
- Study coordinator: Buket MERAL, Msc
- Email: buketguvenir@hotmail.com
- Phone: +90 4622300476
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.