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The Safety and Efficacy of Fibrinolysis in Patients With an Indwelling Pleural Catheter for Multi-loculated Malignant Pleural Effusion.

Primary Purpose

Pleural Effusion, Cancer, Lung

Status
Withdrawn
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
tPA standard dosage
tPA low dosage
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pleural Effusion

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Malignant Pleural Effusion MPE (either cytology proven or recurrent exudative pleural effusion in the context of histologically proven cancer)
  • Presence of an indwelling pleural catheter (IPC)
  • Nondraining IPC (defined as <50 mL of drainage on the past three drainage attempts) not responding to routine saline flush to assure patency
  • Residual pleural fluid remaining on chest x-ray (CXR) or ultrasound
  • Dyspnea deemed attributable to the effusion (i.e. symptomatic loculations), as assessed by the treating chest physician and using the modified Borg scale
  • Presence of written informed consent from the patient or surrogate

Exclusion Criteria:

  • Age <18
  • Expected survival less than 14 days
  • Known allergy or intolerance to tissue plasminogen activator

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    tPA standard dosage

    tPA low dosage

    Arm Description

    Tissue Plasminogen Activator (tPA) dose of 10 to 25 mg.

    tPA dose of 2.5mg

    Outcomes

    Primary Outcome Measures

    Improvement in patient chest X-ray
    Defined as change in percentage of hemithorax occupied by the pleural opacity on chest X-ray from the baseline chest X-ray to the X-ray at the end of the study protocol.
    Improvement on the modified Borg dyspnea scale after tPA
    Change in modified Borg dyspnea scale obtained at clinic visit where tPA is administered compared to modified Borg dyspnea scale obtained after post-tPA drainage.

    Secondary Outcome Measures

    Time to recurrent loculation
    In patients where tPA restores effective drainage, the time to and rate of patients who experience recurrent ineffective drainage due to loculation
    Rate of pleurodesis
    The rate of patients who are able to have the indwelling pleural catheter removed.
    Improvements in dyspnea using the modified Borg scale
    Change in modified Borg dyspnea scale obtained at initial clinic visit compared to scale at the end of the study protocol.

    Full Information

    First Posted
    September 18, 2018
    Last Updated
    March 3, 2020
    Sponsor
    Yale University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03678090
    Brief Title
    The Safety and Efficacy of Fibrinolysis in Patients With an Indwelling Pleural Catheter for Multi-loculated Malignant Pleural Effusion.
    Official Title
    The Safety and Efficacy of Fibrinolysis in Patients With an Indwelling Pleural Catheter for Multi-loculated Malignant Pleural Effusion: a Prospective Randomized Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2020
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Local IRB recommended IND exemption from FDA, study timeline not able to be met.
    Study Start Date
    December 1, 2018 (Anticipated)
    Primary Completion Date
    February 28, 2020 (Actual)
    Study Completion Date
    February 28, 2020 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Yale University

    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
    The safety and efficacy of fibrinolysis in patients with an indwelling pleural catheter for multi-loculated malignant pleural effusion.
    Detailed Description
    Malignant pleural effusion (MPE) is a condition where fluid accumulates in the chest (pleural space) due to the presence of cancer. The malignancy may is usually metastatic from the lung, breast, or elsewhere and the presence of a MPE usually causes significant morbidity, particularly shortness of breath. Once a MPE develops, the patient's disease cannot be cured, but symptoms of dyspnea can be palliated. Malignant effusions usually recur after thoracentesis, a procedure to remove the fluid. Upon recurrence, patients usually undergo placement of an indwelling pleural catheter (IPC). This is a small tube that drains fluid from inside the chest into a bottle to be discarded. It is very effective at treating shortness of breath and is safe. On occasion, these catheters stop functioning, leading to an increase in the effusion again. This may be due to small amounts of blood or debris such as fibrin that clog the catheter, or it may be related to the pleural fluid becoming too thick to drain. Medication, namely tissue plasminogen activator (tPA), can be placed inside the catheter to promote drainage. With simple clogging, the tPA acts like "Draino." For fluid that has become too thick and pleural effusions that won't drain due to loculations, the tPA helps dissolve debris in the pleural fluid to promote drainage. Without this drainage, patients remain impaired due to shortness of breath related to the fluid. tPA is effective at draining the fluid when debris has clogged the catheter or the pleural space. However, the exact dosing is unknown. For "simple" clogging, small doses may be used. When extensive loculations are present, large doses may be required to help the patient. Two retrospective studies have looked at very small doses of tPA placed through the IPC with the goal of breaking up the clogs in the catheter itself. These studies used between 2 and 5 mg of tPA.1,2 At Yale-New Haven Hospital, 25 mg has typically been used due to historical preference. It is unknown whether high doses of tPA improve its therapeutic efficacy. The investigators hypothesize that higher dose fibrinolysis with 25mg of tPA (compared with 2.5 mg) will provide more effective clearance of fluid loculations, resulting in improved radiographic appearance and less shortness of breath without an increased risk of complications, such as bleeding.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Pleural Effusion, Cancer, Lung

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare Provider
    Masking Description
    double blinded
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    tPA standard dosage
    Arm Type
    Active Comparator
    Arm Description
    Tissue Plasminogen Activator (tPA) dose of 10 to 25 mg.
    Arm Title
    tPA low dosage
    Arm Type
    Experimental
    Arm Description
    tPA dose of 2.5mg
    Intervention Type
    Drug
    Intervention Name(s)
    tPA standard dosage
    Other Intervention Name(s)
    tissue plasminogen activator
    Intervention Description
    Tissue plasminogen activator 25mg dosage
    Intervention Type
    Drug
    Intervention Name(s)
    tPA low dosage
    Other Intervention Name(s)
    tissue plasminogen activator
    Intervention Description
    Tissue plasminogen activator 2.5mg
    Primary Outcome Measure Information:
    Title
    Improvement in patient chest X-ray
    Description
    Defined as change in percentage of hemithorax occupied by the pleural opacity on chest X-ray from the baseline chest X-ray to the X-ray at the end of the study protocol.
    Time Frame
    up to 40 days
    Title
    Improvement on the modified Borg dyspnea scale after tPA
    Description
    Change in modified Borg dyspnea scale obtained at clinic visit where tPA is administered compared to modified Borg dyspnea scale obtained after post-tPA drainage.
    Time Frame
    up to 40 days
    Secondary Outcome Measure Information:
    Title
    Time to recurrent loculation
    Description
    In patients where tPA restores effective drainage, the time to and rate of patients who experience recurrent ineffective drainage due to loculation
    Time Frame
    up to 90 days
    Title
    Rate of pleurodesis
    Description
    The rate of patients who are able to have the indwelling pleural catheter removed.
    Time Frame
    up to 90 days
    Title
    Improvements in dyspnea using the modified Borg scale
    Description
    Change in modified Borg dyspnea scale obtained at initial clinic visit compared to scale at the end of the study protocol.
    Time Frame
    up to 40 days
    Other Pre-specified Outcome Measures:
    Title
    Subgroup analysis of patients with trapped lung
    Description
    We will also perform subgroup analysis by patients with trapped lung, stratification by primary tumor type, and stratification by the LENT score (a validated prognostic score for predicting mortality in patients with MPE).
    Time Frame
    up to 40 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Malignant Pleural Effusion MPE (either cytology proven or recurrent exudative pleural effusion in the context of histologically proven cancer) Presence of an indwelling pleural catheter (IPC) Nondraining IPC (defined as <50 mL of drainage on the past three drainage attempts) not responding to routine saline flush to assure patency Residual pleural fluid remaining on chest x-ray (CXR) or ultrasound Dyspnea deemed attributable to the effusion (i.e. symptomatic loculations), as assessed by the treating chest physician and using the modified Borg scale Presence of written informed consent from the patient or surrogate Exclusion Criteria: Age <18 Expected survival less than 14 days Known allergy or intolerance to tissue plasminogen activator
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Mark Godfrey, MD
    Organizational Affiliation
    Yale University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    The Safety and Efficacy of Fibrinolysis in Patients With an Indwelling Pleural Catheter for Multi-loculated Malignant Pleural Effusion.

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