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Efficacy of Fibrinolytic Agents in Complicated Pleural Effusion

Primary Purpose

Complicated Pleural Effusion/ Empyema

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Intrapleural Medications
Sponsored by
Beijing Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Complicated Pleural Effusion/ Empyema focused on measuring Pleural empyema, urokinase

Eligibility Criteria

1 Month - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Pleural Empyema diagnostic criteria were based on the "Zhu Futang Practical Pediatrics" (the 7th Edition) and The American Thoracic Society consensus guidelines for management of empyema.

  • Frank pus at tapping or organism demonstrated on Gram stain or culture
  • Pleural fluid pH < 7.2, glucose < 60mg/dl, LDH>1000 IU/ml, protein > 3g/ml and white cells 15,000 cells/mm cube
  • Physical, radiological and laboratory signs accompanying the relevant clinical picture

Inclusion Criteria:

  • Previously healthy child with age between 1 month to 18 years
  • Admitted with diagnosis of Pleural empyema requiring chest tube insertion and fibrinolytics (as judged by the attending physician) with the following criteria:

I. Pneumonia with pleural empyema based on chest ultrasound and CT scan. II. Need for further intervention based on clinical criteria (persistent fever despite antibiotics for at least 48 hours, significant respiratory distress, tachypnea or hypoxia as a result of pleural empyema.

Exclusion Criteria:

Subject will be excluded if she or he has one of the followings:

  • Empyema as result of tuberculosis, fungus or noninfectious causes (e.g. malignancy)
  • Known coagulation impairment
  • Suspected allergy to urokinase
  • Child has already undergone drainage procedure or drug was used in 30 days (e.g.

chest tube or VATS

  • Chronic lung diseases or other chronic illnesses (e.g. Immunodeficiency, neurological impairment possible)
  • Significant thoracic trauma in last 2 months
  • Severe arterial hypertension
  • Presence of Pneumothorax before treatment (i.e. bronchopleural fistula)
  • Pregnancy
  • Breast feeding
  • Poor compliance
  • Contraindication in the presence of fibrinolytic agent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    use of fibrinolytic agent

    no use of any drug

    Arm Description

    Chest tube drainage with intrapleural urokinase instillation 1000 IU/ml

    Chest tube drainage

    Outcomes

    Primary Outcome Measures

    Length of hospital stay

    Secondary Outcome Measures

    Days of fever after chest tube insertion
    Duration of drainage
    Complications
    number of participants changed to open thoracotomy
    Failure rate

    Full Information

    First Posted
    October 7, 2018
    Last Updated
    November 5, 2018
    Sponsor
    Beijing Children's Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03716375
    Brief Title
    Efficacy of Fibrinolytic Agents in Complicated Pleural Effusion
    Official Title
    A Randomized Controlled Study of Fibrinolytic Treatment for Purulent Pleural Effusion in Children
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    November 2018 (Anticipated)
    Primary Completion Date
    April 30, 2019 (Anticipated)
    Study Completion Date
    April 30, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Beijing Children's Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Intrapleural administration of fibrinolytic therapy, urokinase in parapneumonic effusion and empyema has been shown to decrease the need for surgical intervention and length of hospital stay. Pleural adhesions are easily formed in the early stages of empyema and the thickening of the pleural causes subsequent treatment difficulties. The goal of this study was to observe and compare the efficacy of treatment in empyema patients with urokinase and chest drainage or with chest drainage or with chest tube drainage alone so as to provide evidence for guiding clinical treatment.
    Detailed Description
    Empyema, a collection of pus in the pleural space has been continuously associated with morbidity and mortality rates of 10-20%. Increase in the incidence of empyema with change in pattern of disease and the causative organism has demonstrated a challenge in the diagnosis and treatment. In the recent years many studies and clinical trials have been done among adults and children regarding the optimal empyema treatment and its efficacy and some are still in the process of further study. Appropriate treatment according to the three stages of empyema (i.e. exudative stage, fibropurulent stage and organizing stage) has constantly been under frequent research, finding which treatment is more effective (i.e. antibiotics, chest tube drainage, intrapleural fibrinolytics, VATS and decortication alone in combination) and when is the proper time for intervention. Intrapleural instillation of urokinase was initially described in 1994 on pediatric population and since then lots of studies have been reported. Therefore, the investigators conducted a randomized controlled study with relevant inclusion and exclusion criteria to assess the success rate of intrapleural urokinase administration among the patients with Complicated Pleural Effusion (CPE) / empyema comparing it with drainage alone. All case patients in this study received antibiotic empirically or with sensitivity when microbiological tests available, chest tube drainage along with urokinase intrapleural therapy or drainage alone for treatment of CPE/empyema. Patients will be randomized into two groups: one is chest tube drainage and intrapleural fibrinolytic agent and another is chest tube drainage alone. The group with intrapleural fibrinolytic agent will receive urokinase 10ml of 1000 IU/ml in children aged less than or equal to 1 year or 40ml of 1000 IU/ml in children aged more than 1 year and the other group with drainage alone. The first instillation of the agent is done at the time of chest tube insertion of 12Fr or 14Fr tube, after instillation the chest tube is closed for 4 hours. The chest tube is then unclamped after 4 hours and connected to the suction system with pressure of -20cm H2O for 8 hours and the process is repeated every 12 hourly. The procedure was done for 3 consecutive days and was evaluated with daily chest X-ray and followed chest tube removal when the drainage was less than 40ml/day or according to the clinical and radiological response of patients with treatment. The trial is being done for 12 months with 80 participants taken from one center, Beijing children´s Hospital. The aim of this study is to evaluate difference among intrapleural urokinase as the initial treatment for children with pleural empyema against chest tube drainage alone. Length of hospital stay, number of days chest tube drainage, number of days of fever after tube insertion, complications such bleeding, chest pain will be compared between the two groups.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Complicated Pleural Effusion/ Empyema
    Keywords
    Pleural empyema, urokinase

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    80 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    use of fibrinolytic agent
    Arm Type
    Experimental
    Arm Description
    Chest tube drainage with intrapleural urokinase instillation 1000 IU/ml
    Arm Title
    no use of any drug
    Arm Type
    No Intervention
    Arm Description
    Chest tube drainage
    Intervention Type
    Drug
    Intervention Name(s)
    Intrapleural Medications
    Intervention Description
    urokinase
    Primary Outcome Measure Information:
    Title
    Length of hospital stay
    Time Frame
    2 weeks
    Secondary Outcome Measure Information:
    Title
    Days of fever after chest tube insertion
    Time Frame
    3 to 4 days
    Title
    Duration of drainage
    Time Frame
    2 weeks
    Title
    Complications
    Description
    number of participants changed to open thoracotomy
    Time Frame
    2weeks
    Title
    Failure rate
    Time Frame
    2weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    1 Month
    Maximum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Pleural Empyema diagnostic criteria were based on the "Zhu Futang Practical Pediatrics" (the 7th Edition) and The American Thoracic Society consensus guidelines for management of empyema. Frank pus at tapping or organism demonstrated on Gram stain or culture Pleural fluid pH < 7.2, glucose < 60mg/dl, LDH>1000 IU/ml, protein > 3g/ml and white cells 15,000 cells/mm cube Physical, radiological and laboratory signs accompanying the relevant clinical picture Inclusion Criteria: Previously healthy child with age between 1 month to 18 years Admitted with diagnosis of Pleural empyema requiring chest tube insertion and fibrinolytics (as judged by the attending physician) with the following criteria: I. Pneumonia with pleural empyema based on chest ultrasound and CT scan. II. Need for further intervention based on clinical criteria (persistent fever despite antibiotics for at least 48 hours, significant respiratory distress, tachypnea or hypoxia as a result of pleural empyema. Exclusion Criteria: Subject will be excluded if she or he has one of the followings: Empyema as result of tuberculosis, fungus or noninfectious causes (e.g. malignancy) Known coagulation impairment Suspected allergy to urokinase Child has already undergone drainage procedure or drug was used in 30 days (e.g. chest tube or VATS Chronic lung diseases or other chronic illnesses (e.g. Immunodeficiency, neurological impairment possible) Significant thoracic trauma in last 2 months Severe arterial hypertension Presence of Pneumothorax before treatment (i.e. bronchopleural fistula) Pregnancy Breast feeding Poor compliance Contraindication in the presence of fibrinolytic agent
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Xu Baoping, MD, PhD
    Phone
    +861059616308
    Email
    xubaopingbch@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Xu Baoping, MD, PhD
    Organizational Affiliation
    Beijings Children´s Hospital of Capital Medical University, China
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    26835359
    Citation
    Shirota C, Uchida H. Initial treatment of septated parapneumonic empyema with drainage plus fibrinolytic agents is equally effective as video-assisted thoracoscopic surgery, and is suitable as first-line therapy. Transl Pediatr. 2015 Jan;4(1):41-4. doi: 10.3978/j.issn.2224-4336.2015.02.01.
    Results Reference
    result
    PubMed Identifier
    20304453
    Citation
    Stefanutti G, Ghirardo V, Barbato A, Gamba P. Evaluation of a pediatric protocol of intrapleural urokinase for pleural empyema: a prospective study. Surgery. 2010 Sep;148(3):589-94. doi: 10.1016/j.surg.2010.01.010. Epub 2010 Mar 20.
    Results Reference
    result
    PubMed Identifier
    20736395
    Citation
    Walker W, Wheeler R, Legg J. Update on the causes, investigation and management of empyema in childhood. Arch Dis Child. 2011 May;96(5):482-8. doi: 10.1136/adc.2009.165357. Epub 2010 Aug 24.
    Results Reference
    result

    Learn more about this trial

    Efficacy of Fibrinolytic Agents in Complicated Pleural Effusion

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