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Withdrawn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
About this trial
This is an interventional treatment trial for Pleural Effusion
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
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
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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