Clinical Trials Directory

Trials / Completed

CompletedNCT00854815

Irrigation Versus No Irrigation for Perforated Appendicitis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
220 (estimated)
Sponsor
Children's Mercy Hospital Kansas City · Academic / Other
Sex
All
Age
1 Month – 17 Years
Healthy volunteers
Not accepted

Summary

The purpose is to quantify the effect of irrigation during laparoscopic appendectomy for perforated appendicitis.

Detailed description

This will be a prospective, randomized clinical trial involving patients who present to the hospital with perforated appendicitis. This will be a definitive study. Power calculation was based on abscess rate in the previous prospective study. An unacceptable abscess rate needed to be chosen. Our current rate is 20%, or one-fifth of the patients. If this were to increase by 15%, it would place just over one third of the patients at risk which would be unacceptable. This is comparable to the 36% rejection level we used for the previous IRB approved trial (#07 02-031). Using a delta of 0.15 with alpha of 0.05 and power of 0.8, the sample size is 109 patients in each arm. Therefore we will anticipate enrolling 220. Subjects will be those children who are found to have severe inflammatory changes on imaging or a high clinical suspicion of perforation. Permission will be obtained from parents prior to the operation. All of these children will be under duress prior to randomization, therefore we request waiving assent as we have done with the previous perforated appendicitis studies. The final decision to include a child in the study will made after perforation has been visually confirmed during surgery. Perforation will be defined as an identifiable hole in the appendix or stool in the abdomen. The randomization assignment will be made known at the initiation of the operation, and confirmation of perforation will confirm the patient will utilize the next randomization slot. The irrigation group will have suction irrigator set up with a 1 liter bag of normal saline. The surgeon must use at least 500 ml of this bag but may use as much as they choose. The no irrigation group will have the suction irrigator set up without the saline attachment. This will leave them with the capacity for suction only. Since several suction devices exist, this will assure the same type of suction for both groups. After the operation, both groups will be managed in the same manner. When the patient is tolerating a regular diet, on oral pain medication and has been afebrile for over 12 hours, they will be discharged on oral antibiotics to complete a course of 7 days. If they stay until the 5th post-operative day, a white blood cell count will be checked, which if it is normal, they will be discharged to home without antibiotics. This is standard post-operative care as delineated by our previous prospective, randomized.

Conditions

Interventions

TypeNameDescription
PROCEDUREIrrigationIrrigation of the area with at least 500ml NS using the power suction/irrigator
PROCEDURENo IrrigationSuction only using suction/irrigator

Timeline

Start date
2008-12-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2009-03-03
Last updated
2012-08-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00854815. Inclusion in this directory is not an endorsement.