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Single Incision Laparoscopic Surgery (SILS) Versus Laparoscopic Appendectomy

Single Incision Versus Standard Laparoscopic Appendectomy for Non-Perforated Appendicitis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00981136
Enrollment
360
Registered
2009-09-22
Start date
2009-08-31
Completion date
2011-12-31
Last updated
2013-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Appendicitis

Keywords

Appendicitis, Appendectomy, Children, Laparoscopic, SILS

Brief summary

This is a prospective trial of single incision versus standard 3-port laparoscopic appendectomy. The hypothesis is that there may a difference in wound infection rates, operative time, doses of analgesics post-operatively, and patient/parent perception of scars.

Detailed description

This is a prospective, randomized clinical trial involving patients who present to the hospital with non-perforated appendicitis. We will offer enrollment to several institutions provided they receive institutional approval. There are likely several parameters that will show small differences between groups, and this study will precisely quantify them to allow for adequate consultation from surgeons to families dealing with acute appendicitis. One theoretical concern over the SILS approach is that the exposure of the appendix to the wound could increase the rate of infectious complications; therefore, this is the primary outcome variable. The documented rate of infectious complications at our institution in patients with non-perforated appendicitis is 0.6%. An unacceptable and clinically relevant rise to 5% may curtail enthusiasm for the new technique. Using a power of 0.9 with an α of 0.05, the sample size is 360 total patients or 180 in each arm. After the procedure, both groups will be managed in the same manner per routine care. They will be discharged when tolerating a regular diet and their pain is well-controlled on oral pain medication. Cosmetic scores will be obtained at 6 weeks and 6 months.

Interventions

A single incision through the umbilicus to remove the appendix

Standard 3 port laparoscopic appendectomy with intracorporeal stapling

Sponsors

Children's Mercy Hospital Kansas City
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

* Children under 18 years * Non-perforated appendicitis

Exclusion criteria

* Perforated appendicitis as identified as a hole in the appendix for fecalith in the abdomen

Design outcomes

Primary

MeasureTime frame
Post-operative infection6 weeks

Secondary

MeasureTime frame
Operative time1 day
Cosmetic scores6 months
Doses of analgesic3 days
Surgeon perception of difficulty1 day
Hospital/operative charges1 week
Length of Hospitalization1 week

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026