Clinical Trials Directory

Trials / Completed

CompletedNCT03524573

(D)Elayed vs. (E)Arly (L)Aparoscopic (A)Ppendectom(Y)

Delayed vs. Early Laparoscopic Appendectomy : A Randomized Controlled Trial (The DELAY Trial)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
127 (actual)
Sponsor
Queen's University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The DELAY Trial will compare immediate (\< 6 hours from decision to operate) to delayed (Surgery to take place the following morning) appendectomy in adult patients presenting to the emergency department with suspected acute appendicitis. The primary outcome will be 30 day postoperative complications.

Detailed description

This randomized controlled trial is designed to assess the effect of timing of surgery on surgical complications in patients undergoing appendectomy for acute appendicitis at one of two participating institutions. Early appendectomy in patients diagnosed with acute appendicitis has been a mainstay of treatment. Timely intervention is recommended to avoid the risks associated with perforated appendicitis, which has been shown to increase the risk of post-operative complications compared to non-perforated appendicitis. However, some studies have suggested that delaying appendectomy does not increase complications. Several studies have also assessed the safety of nighttime operating with conflicting results. Some suggest that delaying surgery until daytime is safe. This study is a prospective, randomized controlled trial with blinding of the outcome assessors. Eligible participants will be adult patients diagnosed with acute appendicitis with an expected operative start time between 2000-0400. Patients randomized to the intervention group will have delayed surgery after 0530 the following morning to avoid nighttime operating. Patients randomized to the control group will receive immediate surgery within 6 hours of the decision to operate. The follow up period will be a minimum of 30 days. Independent outcome assessors will assess patients during their postoperative course in hospital as well as in the outpatient follow up clinic. The primary outcome for this study is complication occurring within 30 days of surgery. Complication includes any of the following: mortality, readmission to hospital, emergency department (ED) visit, percutaneous drain insertion, reoperation, prolonged hospital stay greater than 7 days, and a predefined list of postoperative complications. Secondary outcomes include perforated appendicitis, operative time, and length of stay.

Conditions

Interventions

TypeNameDescription
PROCEDUREAppendectomyAppendectomy is the surgical removal of the appendix.

Timeline

Start date
2018-11-05
Primary completion
2023-03-30
Completion
2023-03-30
First posted
2018-05-15
Last updated
2023-11-18

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT03524573. Inclusion in this directory is not an endorsement.

(D)Elayed vs. (E)Arly (L)Aparoscopic (A)Ppendectom(Y) (NCT03524573) · Clinical Trials Directory