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Clinical Trials/NCT06059365
NCT06059365
Not yet recruiting
Not Applicable

Randomized Clinical Trial to Test the Efficacy and Safety of Outpatient Clinical Management of Urgent Laparoscopic Appendectomy in Complicated Acute Appendicitis

HJ230 sites92 target enrollmentNovember 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Appendicitis
Sponsor
HJ23
Enrollment
92
Primary Endpoint
length of hospital stay (LHS)
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study is to evaluate the safety and efficacy of outpatient management of complicated acute appendicitis. For this purpose, a randomized clinical trial was designed. Selected patients who have undergone surgery for acute appendicitis are randomized into two groups. One group with hospitalization and another group without admission.

Detailed Description

The aim of this study is to evaluate the efficacy and safety of outpatient management of laparoscopic appendicectomy in complicated acute appendicitis. This was a single center randomized controlled clinical trial consisting in 2 treatment groups. Patients were recruited in University Hospital of Tarragona Joan XXIII of Spain. All patients admitted in the emergency department at University Hospital of Tarragona Joan XXIII with acute appendicitis diagnosis were likely to enter in the study. All patients who met the inclusion criteria and none of the exclusion criteria were admitted to the study for emergency surgery. In order to avoid the biases a unique anesthetic and surgical protocol were established for both groups. Once Laparoscopic appendicectomy was performed the patients were randomly assigned to the hospitalization group or outpatient group. Patients in the hospitalization group were admitted in the hospitalization ward. Patients in the outpatient group were referred to the day-surgery unit where they were discharged according to ALDRETE criteria. The primary endpoint was the length of hospital stay (LHS). The length of hospital stay was calculated from the day and hour of admission in the surgical area to the day and hour of discharge, based on the hours of hospital stay. Secondary endpoints included the failures of the outpatient management, readmissions and the hospitals cost

Registry
clinicaltrials.gov
Start Date
November 1, 2023
End Date
November 1, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
HJ23
Responsible Party
Principal Investigator
Principal Investigator

Jordi Elvira Lopez

MD PhD

HJ23

Eligibility Criteria

Inclusion Criteria

  • patients over 18 years old
  • ASA classification (American Society of Anesthesiologists) less than or equal to 3
  • patients who live accompanied in a home at a maximum distance of 30 minutes from the hospital and an adequate cognitive capacity.

Exclusion Criteria

  • pregnancy or breastfeeding
  • complicated Acute Appendicitis
  • surgical management performed in more 90 minutes

Outcomes

Primary Outcomes

length of hospital stay (LHS)

Time Frame: up to 5 days

The length of hospital stay (LHS) was calculated from the date and time of urgent appendectomy surgery to the date and time of hospital discharge, based on the hours of hospital stay (assessed up to 5 days)

Secondary Outcomes

  • failures of the outpatient management(assessed up to 30 days)
  • readmissions(assessed up to 30 days)
  • hospitals cost(through study completion, an average of 1 year)

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