Clinical Trials Directory

Trials / Completed

CompletedNCT05962320

Effect of Modified ERAS Protocol on Clinical Outcomes in Pediatric Patients With Appendectomy

Effect of Enhanced Recovery After Surgery Protocol Based Care on Patient Outcomes in Children With Appendicitis: a Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
82 (actual)
Sponsor
Karadeniz Technical University · Academic / Other
Sex
All
Age
6 Years – 17 Years
Healthy volunteers
Not accepted

Summary

Acute appendicitis is the most common abdominal emergency with more than 15 million cases reported worldwide. Although appendectomy is considered a safe surgical procedure, the incidence of complications is up to 10%. The Enhanced Recovery After Surgery (ERAS) has developed guidelines to improve postoperative patient outcomes. The protocol, which consists of more than 20 interventions in the preoperative, intraoperative and postoperative periods, shows that early discharge can be possible with multidisciplinary care given to surgical patients without risking patient safety.

Detailed description

Appendicitis is a common clinical condition and often requires emergency treatment. Although appendectomy is a safe surgical procedure, there is a risk of complications. Pain is common, especially in the postoperative period, and the lack of care management leads to delayed mobilization and oral intake, delayed recovery and prolonged length of hospital stay. However, pain, nausea-vomiting, thirst, fear and stress could be managed with perioperative care. In addition, it is reported that the care provided based on the ERAS protocol shortens the length of hospital stay. In this respect, the aim of this study was to investigate the effect of ERAS protocol-based care on the length of hospital stay of children who were planned to undergo appendectomy. Postoperative pain level, stress and fear level, time to first mobilization, flatulence, defecation and oral intake, nausea, thirst were the secondary outcomes of this study.

Conditions

Interventions

TypeNameDescription
OTHEREducation and counsellingEducation and counselling of patients and their parents
OTHERAvoiding the use of nasogastric catheters, drains and urinary cathetersAvoiding the use of nasogastric catheters, drains and urinary catheters or/and removing them as early as possible
OTHERStimulation of intestinal motility in the postoperative periodStimulation of intestinal motility in the postoperative period
OTHERInitiation of oral intake in the early postoperative periodInitiation of oral intake in the early postoperative period
OTHEREarly removal of the patient by reducing postoperative IV fluid infusionEarly removal of the patient by reducing postoperative IV fluid infusion
OTHERInitiation of early mobilization of the patient in the postoperative periodInitiation of early mobilization of the patient in the postoperative period
OTHERReducing opioid use and ensuring pain managementReducing opioid use and ensuring pain management
OTHERImplement nausea and vomiting prophylaxisImplement nausea and vomiting prophylaxis
OTHERManagement of thirstyManagement of thirsty
OTHERManagement of fear and stressUse of recommended non-pharmacological interventions in the management of fear and stress

Timeline

Start date
2023-10-01
Primary completion
2024-05-01
Completion
2024-05-31
First posted
2023-07-27
Last updated
2025-10-03

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05962320. Inclusion in this directory is not an endorsement.