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Effectiveness of Doxycycline for Treating Pleural Effusions Related to Cancer in an Outpatient Population (OPUS)

Primary Purpose

Malignant Pleural Effusion

Status
Unknown status
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Doxycycline
normal saline
Sponsored by
Ottawa Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malignant Pleural Effusion focused on measuring Malignant Pleural Effusion, Doxycycline, Pleurodesis, Pleurx catheter

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Presence of symptomatic and moderate sized (>1/3 of hemithorax) MPE
  2. Persistent malignant pleural effusion that is free-flowing
  3. Symptomatic improvement after therapeutic thoracentesis
  4. Life expectancy of at least three months (duration of study follow-up)
  5. 90% radiographic apposition of parietal and visceral pleura
  6. Residence within 30 minute radius from The Ottawa Hospital

Exclusion Criteria:

  1. Previous lobectomy or pneumonectomy on affected side
  2. Multiple loculations
  3. Trapped or entrapped lung
  4. Untreated pleural infection
  5. Abnormal coagulation profile (INR>1.5 and / or platelet count <50 x 10*9/L)
  6. Planned intrapleural chemotherapy (however participants may receive concomitant systemic chemotherapy, mediastinal radiation therapy or steroids)
  7. Life expectancy less than 3 months
  8. Multiple co-morbidities limiting out-patient management of pleural effusion
  9. Tetracycline / Doxycycline allergy

Sites / Locations

  • Ottawa HospitalRecruiting
  • The Ottawa HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Doxycycline

Normal Saline

Arm Description

Pleurx insertion with injection of 500mg of doxycycline in 50cc of normal saline.

Pleurx insertion with placebo injection of 50cc of normal saline

Outcomes

Primary Outcome Measures

Time to pleurodesis
measured in days after Pleurx catheter insertion up to 90 days

Secondary Outcome Measures

Pleurodesis rates at 90 days post Pleurx insertion
defined by the BTS guidelines, where complete pleurodesis is defined as lack of fluid re-accumulation, allowing for removal of the pleural catheter. Failed pleurodesis is defined as re-accumulation of fluid and symptoms requiring repeated pleural procedures
Number of participants with adverse events
Most common complications include: pleural infection / cellulitis, pain, catheter obstruction and symptomatic loculated effusion. Other adverse events will also be collected.
Effects on pulmonary function
Pulmonary Function testing will be performed prior to and post PleurX catheter insertion and prior to each follow up visit

Full Information

First Posted
June 13, 2011
Last Updated
September 23, 2020
Sponsor
Ottawa Hospital Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT01411202
Brief Title
Effectiveness of Doxycycline for Treating Pleural Effusions Related to Cancer in an Outpatient Population
Acronym
OPUS
Official Title
Outpatient Pleurodesis Using Sclerosants(OPUS):Comparing Doxycycline Pleurodesis to Continued Drainage With the Pleurx Catheter System in the Treatment of Malignant Pleural Effusions in the Outpatient Setting
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 2011 (undefined)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ottawa Hospital Research Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Patients with cancer may experience problems with their breathing due to a fluid accumulation around their lungs called malignant pleural effusion (MPE). This fluid can be drained but draining may not stop the fluid from accumulating again. MPE can cause shortness of breath during activity and at rest leaving patients feeling as though they cannot catch their breath enough to be comfortable. Other symptoms can include pain, cough and weight loss. One way to stop the fluid from accumulating is to create scar tissue between the lung and chest wall so there is no more room for fluid accumulation. This procedure is called pleurodesis. Pleurodesis is the standard of care at most centres across Canada. This procedure is done by injecting a drug into the space between the lung and chest wall through a catheter, Doxycycline is one of the drugs currently used for this purpose. Traditionally, patients are admitted for pleurodesis, mostly because the size of the catheter used to inject the medication is very large but also because of the potential complications that can happen with these larger chest tubes. At our centre, most patients with MPE are managed at home with a smaller sized catheter known as a Pleurx catheter. The Pleurx catheter allows patients to remain at home for treatment and trained staff come into the home to both drain the MPE and monitor the patient. Sometimes, patients experience pleurodesis through use of the Pleurx catheter alone. Pleurodesis with doxycycline can happen faster than with the Pleurx catheter alone. It has been our experience with a limited number of patients that it is safe to perform pleurodesis using the Pleurx catheter for doxycycline injection in an outpatient setting.
Detailed Description
Malignant pleural effusions (MPE) occur in 25 - 50% of malignancies, represent advanced disease and carry with it significant morbidity. It is estimated that 75% of malignant effusions are symptomatic at the time of presentation, with dyspnea being the most common complaint. Cough, weight loss and chest pain may also be presenting symptoms. The diagnosis of MPE often carries with it a poor prognosis with an average survival of 3-9 months. Thus, management of MPE is generally palliative, aimed at alleviating the associated symptoms, while incurring minimal discomfort and disruption of patients activities of daily living. Limiting the number of days spent hospitalized ia also a consideration. Currently, the most common treatment for MPE involves tube thoracostomy and pleurodesis using a sclerosing agent. Use of Doxycycline as a sclerosing agent has been shown to be both safe and efficacious with only minor complications. Traditionally, pleurodesis with Doxycycline has been performed in the inpatient setting. The Pleurx catheter (Cardinal Biomedical) is the only small bore catheter commercially available that has been specifically designed for long term indwelling drainage of MPE. In order to reduce the chance of dislodgement and minimize infection rates, it is tunnelled under the skin for approximately 5 cm before entering the pleural space. These indwelling catheters can provide excellent symptom control and have also been associated with spontaneous pleurodesis rates comparable to many chemical pleurodesis rates. Pleurx has been compared to inpatient doxycycline pleurodesis via chest tube with no difference in survival, safety or efficacy noted. However, hospital stay was significantly shorter in the Pleurx group, 1 day versus 6.5 days. The aim of this study is to determine the effectiveness of outpatient pleurodesis, using doxycycline administered via Pleurx catheter. This will be a randomized clinical trial comparing the time to pleurodesis in patients with malignant pleural effusion receiving doxycycline + Pleurx catheter versus Pleurx catheter alone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malignant Pleural Effusion
Keywords
Malignant Pleural Effusion, Doxycycline, Pleurodesis, Pleurx catheter

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Doxycycline
Arm Type
Experimental
Arm Description
Pleurx insertion with injection of 500mg of doxycycline in 50cc of normal saline.
Arm Title
Normal Saline
Arm Type
Placebo Comparator
Arm Description
Pleurx insertion with placebo injection of 50cc of normal saline
Intervention Type
Drug
Intervention Name(s)
Doxycycline
Intervention Description
One time injection 500mg of powdered doxycycline reconstituted with 50cc of normal saline via Pleurx catheter
Intervention Type
Other
Intervention Name(s)
normal saline
Intervention Description
One time injection of normal saline (placebo) into Pleurx catheter
Primary Outcome Measure Information:
Title
Time to pleurodesis
Description
measured in days after Pleurx catheter insertion up to 90 days
Time Frame
up to 90 days post PleurX insertion
Secondary Outcome Measure Information:
Title
Pleurodesis rates at 90 days post Pleurx insertion
Description
defined by the BTS guidelines, where complete pleurodesis is defined as lack of fluid re-accumulation, allowing for removal of the pleural catheter. Failed pleurodesis is defined as re-accumulation of fluid and symptoms requiring repeated pleural procedures
Time Frame
90 days post Pleurx insertion
Title
Number of participants with adverse events
Description
Most common complications include: pleural infection / cellulitis, pain, catheter obstruction and symptomatic loculated effusion. Other adverse events will also be collected.
Time Frame
90 days post Pleurx insertion
Title
Effects on pulmonary function
Description
Pulmonary Function testing will be performed prior to and post PleurX catheter insertion and prior to each follow up visit
Time Frame
90 days post Pleurx insertion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Presence of symptomatic and moderate sized (>1/3 of hemithorax) MPE Persistent malignant pleural effusion that is free-flowing Symptomatic improvement after therapeutic thoracentesis Life expectancy of at least three months (duration of study follow-up) 90% radiographic apposition of parietal and visceral pleura Residence within 30 minute radius from The Ottawa Hospital Exclusion Criteria: Previous lobectomy or pneumonectomy on affected side Multiple loculations Trapped or entrapped lung Untreated pleural infection Abnormal coagulation profile (INR>1.5 and / or platelet count <50 x 10*9/L) Planned intrapleural chemotherapy (however participants may receive concomitant systemic chemotherapy, mediastinal radiation therapy or steroids) Life expectancy less than 3 months Multiple co-morbidities limiting out-patient management of pleural effusion Tetracycline / Doxycycline allergy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rosalie Labelle, MSc
Phone
613-737-8899
Ext
75256
Email
rolabelle@toh.on.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
K. Amjadi, MD, FRCPC
Organizational Affiliation
Ottawa Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ottawa Hospital
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L6
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kayvan Amjadi, MD
Facility Name
The Ottawa Hospital
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H8L6
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
K. Amjadi, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
N. Voduc, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Effectiveness of Doxycycline for Treating Pleural Effusions Related to Cancer in an Outpatient Population

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