Initial Versus Delayed Operation for Treatment of Complicated Appendicitis In Children
Primary Purpose
Perforated Appendicitis
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Initial appendectomy
Interval appendectomy
Sponsored by
About this trial
This is an interventional treatment trial for Perforated Appendicitis focused on measuring appendicitis, perforated, children
Eligibility Criteria
Inclusion Criteria:children
- Age 2-17 with a diagnosis of perforated appendicitis
Exclusion Criteria:
- Age <2 and >18
- Pregnancy
- Immunocompromise
Sites / Locations
- Mott Childrens Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Initial appendectomy
Interval appendectomy
Arm Description
children with complicated appendicitis will undergo initial appendectomy
children with complicated appendicitis will undergo initial antibiotic treatment followed by an interval appendectomy
Outcomes
Primary Outcome Measures
cost effectiveness
Secondary Outcome Measures
Full Information
NCT ID
NCT00540189
First Posted
October 4, 2007
Last Updated
December 16, 2016
Sponsor
University of Michigan
1. Study Identification
Unique Protocol Identification Number
NCT00540189
Brief Title
Initial Versus Delayed Operation for Treatment of Complicated Appendicitis In Children
Official Title
Initial Versus Delayed Operation for Treatment of Complicated Appendicitis In Children
Study Type
Interventional
2. Study Status
Record Verification Date
December 2016
Overall Recruitment Status
Terminated
Why Stopped
Unable to adequatly recruit
Study Start Date
May 2008 (undefined)
Primary Completion Date
January 2010 (Actual)
Study Completion Date
January 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
To determine the most cost effective way to treat children with perforated appendicitis we will randomize all children presenting with perforated appendicitis to initial operation, with in 24 hours of admission, or to initial antibiotics, with or without percutaneous drainage, and subsequent interval appendectomy after 8 weeks. Our outcomes will include cost, complications, length of stay, and quality of life measures.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Perforated Appendicitis
Keywords
appendicitis, perforated, children
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
23 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Initial appendectomy
Arm Type
Other
Arm Description
children with complicated appendicitis will undergo initial appendectomy
Arm Title
Interval appendectomy
Arm Type
Other
Arm Description
children with complicated appendicitis will undergo initial antibiotic treatment followed by an interval appendectomy
Intervention Type
Procedure
Intervention Name(s)
Initial appendectomy
Intervention Type
Procedure
Intervention Name(s)
Interval appendectomy
Primary Outcome Measure Information:
Title
cost effectiveness
Time Frame
3 months post entry into the study
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:children
Age 2-17 with a diagnosis of perforated appendicitis
Exclusion Criteria:
Age <2 and >18
Pregnancy
Immunocompromise
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven W Bruch, MD, MSc
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mott Childrens Hospital
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Initial Versus Delayed Operation for Treatment of Complicated Appendicitis In Children
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