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Safety and Efficacy Study of Single Port Laparoscopic Appendectomy in Acute Appendicitis

Prospective, Randomized Study of Single Port and Conventional Laparoscopic Appendectomy in Acute Appendicitis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01007318
Enrollment
194
Registered
2009-11-04
Start date
2009-12-31
Completion date
2016-02-29
Last updated
2020-09-07

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

Conditions

Appendicitis

Brief summary

The aim of this study is to investigate the safety and efficacy of single port laparoscopic appendectomy compared with conventional laparoscopic appendectomy in adults with acute appendicitis.

Detailed description

Laparoscopic appendectomy improved the postoperative functional outcomes in the treatment of acute appendectomy. In addition, recently single port laparoscopic surgery was introduced in the laparoscopy-dedicated center. When compared with conventional 3 port laparoscopic appendectomy, single port laparoscopic appendectomy was expected to be less painful, more rapid recovery of bowel function, and better cosmetic. In this prospective randomized trial, we tried to investigate the superiority of this new technique in adult patients with acute appendectomy.

Interventions

PROCEDURESingle port laparoscopic appendectomy

Single port through the transumbilical 2-cm incision

3 trocars was inserted in infraumbilical, left lower quadrant, and suprapubic area

Sponsors

KyungHee University School of Medicine, Korea
CollaboratorUNKNOWN
Kyunghee University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Clinically diagnosed acute appendicitis

Exclusion criteria

* Age less than 7 or more than 75 years old * Gangrenous appendicitis * Combined generalized peritonitis * ASA score more than 3 point * Pregnant women * Cases requiring draining tube

Design outcomes

Primary

MeasureTime frameDescription
Safety1 month30 day morbidity and mortality

Secondary

MeasureTime frameDescription
Efficacy1 dayOperative time

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026