Thoracoscopy Versus Fibrinolysis in Children With Empyema
Primary Purpose
Empyema
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Chest tube with tPA infusion for 3 days
VATS decortication
Sponsored by
About this trial
This is an interventional treatment trial for Empyema focused on measuring thoracoscopy, fibrinolysis, empyema, children
Eligibility Criteria
Inclusion Criteria: Patients less than 18 years of age requiring an intervention for empyema by one of the following: Septation or loculation seen on ultrasound or computed tomography Many white blood cells, bacteria present, or thick viscid purulence identified on pleural tap Exclusion Criteria: Immunodeficiency process Secondary diagnosis or condition that will keep them in the hospital beyond the empyema Existing contraindications to VATS or chest tube.
Sites / Locations
- Children's Mercy Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
1
2
Arm Description
Video assisted thoracoscopic decortication
Fibrinolysis through the chest tube
Outcomes
Primary Outcome Measures
Length of hospitalization after intervention
Secondary Outcome Measures
Days where a maximum temperature was equal to or above 38 degrees C, days of tube drainage, doses of analgesia and days of oxygen requirement, hospital days after intervention, hospital charges after intervention and procedure charges
Full Information
NCT ID
NCT00323531
First Posted
May 8, 2006
Last Updated
May 6, 2008
Sponsor
Children's Mercy Hospital Kansas City
1. Study Identification
Unique Protocol Identification Number
NCT00323531
Brief Title
Thoracoscopy Versus Fibrinolysis in Children With Empyema
Official Title
Thoracoscopy Versus Fibrinolysis in Children With Empyema
Study Type
Interventional
2. Study Status
Record Verification Date
May 2008
Overall Recruitment Status
Completed
Study Start Date
March 2006 (undefined)
Primary Completion Date
October 2007 (Actual)
Study Completion Date
October 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Children's Mercy Hospital Kansas City
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The null hypothesis is that patients receiving either thoracoscopy or fibrinolysis for empyema recover in the same amount of time. Therefore, we will test this by randomizing the next 40 patients who consent to the study to one treatment or the other.
Detailed Description
This will be a single institution, prospective, randomized clinical trial involving patients who are found to have at least a single septation within a pleural effusion as diagnosed by ultrasound or computed tomography. Additionally, patients with a pleural effusion wherein a pleural tap reveals pus as defined by many (> 10,000/mm3 ) white blood cells or positive cultures will be considered. This is intended to be a definitive study.
Power calculations based on the known 4.8 post intervention hospital days after VATS and the estimated 7 post intervention days after fibrinolysis with α = 0.05 and power of 0.8 show the need for 18 patients in each arm. We will intend to recruit 40. This sample size was constructed in consultation with Dr. Steve Simon, and the range of hospital stay in our retrospective experience was utilized. Therefore, this number should represent an adequate power in spite of the known varied level of illness.
One group will undergo thoracoscopy to clean the pleural space and leave a chest tube postoperatively to drainage. The other group will undergo chest tube placement with subsequent infusion of fibrinolytics to dissolve the thick purulent material allowing drainage.
Both groups will have the same antibiotic regimen with the same management algorithm.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Empyema
Keywords
thoracoscopy, fibrinolysis, empyema, children
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
36 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
Video assisted thoracoscopic decortication
Arm Title
2
Arm Type
Experimental
Arm Description
Fibrinolysis through the chest tube
Intervention Type
Procedure
Intervention Name(s)
Chest tube with tPA infusion for 3 days
Other Intervention Name(s)
Fibrinolysis, tPA
Intervention Description
fibrinolysis through the chest tube
Intervention Type
Procedure
Intervention Name(s)
VATS decortication
Other Intervention Name(s)
VATS, pleural debridement
Intervention Description
thoracoscopic decortication
Primary Outcome Measure Information:
Title
Length of hospitalization after intervention
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Days where a maximum temperature was equal to or above 38 degrees C, days of tube drainage, doses of analgesia and days of oxygen requirement, hospital days after intervention, hospital charges after intervention and procedure charges
Time Frame
1 month
10. Eligibility
Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients less than 18 years of age requiring an intervention for empyema by one of the following:
Septation or loculation seen on ultrasound or computed tomography
Many white blood cells, bacteria present, or thick viscid purulence identified on pleural tap
Exclusion Criteria:
Immunodeficiency process
Secondary diagnosis or condition that will keep them in the hospital beyond the empyema
Existing contraindications to VATS or chest tube.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shawn D St. Peter, MD
Organizational Affiliation
Children's Mercy Hospital Kansas City
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Mercy Hospital
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Thoracoscopy Versus Fibrinolysis in Children With Empyema
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