Clinical Trial: Single Incision Versus Standard Laparoscopic Splenectomy

Study Status: Withdrawn
Recruit Status: Withdrawn
Study Type: Interventional

Official Title: Single Incision Versus Standard Laparoscopic Splenectomy

Brief Summary:

This is a prospective trial of single incision versus standard 4-port laparoscopic splenectomy.

The hypothesis is that there may be a difference in wound infection rates, operative time, doses of analgesics post-operatively, and patient/parent perception of scars. However, the technical difficulty is considerable and the primary outcome is operative time which will be expressed in minutes.


Detailed Summary:

This will be a prospective, randomized clinical trial involving patients who present to the hospital with an indication for splenectomy. We will offer enrollment to several institutions provided they reach institutional approval.

This will be a definitive trial design. Based on our operative times with SILS compared with our recent experience in standard laparoscopy, a sample size of 30 patients will give us a power of 0.8 with an α of 0.05. Thus operative time is the primary outcome variable by definition. This is recorded and reported in MINUTES.

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.

Secondary outcome measures include days in the hospital (measured in days), doses of analgesics (measured in doses) and perception of cosmesis as recorded by a scar assessment form which will be filled out by the patient and/or parents at 6 weeks and 6 months. This is a validated quality of life survey with 39 questions and each has 4 categories from best to worst.


Sponsor: Children's Mercy Hospital Kansas City

Current Primary Outcome: Operative time [ Time Frame: 1 day ]

operative time


Original Primary Outcome: Same as current

Current Secondary Outcome:

  • operative complications [ Time Frame: 1 day ]
  • wound complications [ Time Frame: 1 month ]
  • cosmesis [ Time Frame: 6 months ]
  • length of stay [ Time Frame: 1 week ]
  • operative difficulty [ Time Frame: 1 day ]


Original Secondary Outcome: Same as current

Information By: Children's Mercy Hospital Kansas City

Dates:
Date Received: January 11, 2011
Date Started: October 2009
Date Completion: April 2017
Last Updated: February 1, 2017
Last Verified: February 2017