Rational Approach to a Unilateral Pleural Effusion (REPEAT)
Primary Purpose
Lung Neoplasms
Status
Terminated
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Thoracoscopy
VATS (thoracoscopy)
Sponsored by
About this trial
This is an interventional diagnostic trial for Lung Neoplasms focused on measuring Thoracoscopy
Eligibility Criteria
Inclusion Criteria:
- Patients with recurrent pleural effusion of unknown origin after a first pleural tap according to BTS guidelines.
- Indication for thoracoscopy according to BTS guidelines.
- Patients accept further investigation according to Danish and BTS guidelines.
- Have received oral and written consent and agreed.
- At the time of inclusion, above 18 years of age.
Exclusion Criteria:
- Female patients: pregnancy or breastfeeding.
- Lack of language comprehension.
- Legally incompetent patients.
- Life expectancy less than 3 month.
- Contraindications to pleural tissue sampling.
Sites / Locations
- Naestved Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Pleuroscopy
VATS (thoracoscopy)
Arm Description
According to BTS guideline thoracoscopy is the next procedure for patients who remain undiagnosed despite PET-CT and attempts to obtain biopsies. Eligible patients will be randomised to pleuroscopy or VATS. Patients with inconclusive pleuroscopy will proceed to VATS.
According to BTS guideline thoracoscopy is the next procedure for patients who remain undiagnosed despite PET-CT and attempts to obtain biopsies. Eligible patients will be randomised to pleuroscopy or VATS. Patients with inconclusive pleuroscopy will proceed to VATS.
Outcomes
Primary Outcome Measures
Number of patients diagnosed with cancer
(cancer = an unequivocal diagnosis of neoplastic disease; no cancer = clinically benign cause, and improved imaging at 6 month control).
Secondary Outcome Measures
Quality of life
Questionnaire developed to assess the quality of life of cancer patients, QLQC 30
Total costs
calculated as costs patient-related, procedure-related, and overall
Pain
VAS scale
Quality of life
A standardised instrument for use as a measure of health outcome, EuroQol EQ-5D
Full Information
NCT ID
NCT03272087
First Posted
November 5, 2015
Last Updated
December 15, 2020
Sponsor
Naestved Hospital
Collaborators
University of Southern Denmark, Odense University Hospital, Zealand University Hospital, University Hospital, Gentofte, Copenhagen, Bispebjerg Hospital, Rigshospitalet, Denmark
1. Study Identification
Unique Protocol Identification Number
NCT03272087
Brief Title
Rational Approach to a Unilateral Pleural Effusion
Acronym
REPEAT
Official Title
Rational Approach to Unilateral Pleural Effusion in Patients Suspected of Malignancy. Efficacy, Pain, Quality of Life, and Economy
Study Type
Interventional
2. Study Status
Record Verification Date
December 2020
Overall Recruitment Status
Terminated
Why Stopped
Patient inclusion cannot be completed within time limits
Study Start Date
May 2015 (Actual)
Primary Completion Date
December 15, 2020 (Actual)
Study Completion Date
December 15, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Naestved Hospital
Collaborators
University of Southern Denmark, Odense University Hospital, Zealand University Hospital, University Hospital, Gentofte, Copenhagen, Bispebjerg Hospital, Rigshospitalet, Denmark
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Recurrent unilateral, non-infectious pleural exudate is suspicious for primary or secondary pleural malignancy. Both conditions are associated with 5-year survival of 10%. Work-up is difficult, as the pleural surface is large and <33% of pleural malignancies shed malignant cells to the pleural fluid. Even so, additional tissue biopsies are needed for establishing mutation status for targeted therapies.
Optimal imaging to guide tissue sampling is pivotal. PET-CT has higher sensitivity than conventional CT for detecting malignant lesions >10mm. However, no randomised trial has investigated differences in diagnostic accuracy, time-to-diagnosis, or economics. Falsely PET-positive lesions in e.g. colon, however, lead to more derived tests than do CT alone.
Gold standard for pleural tissue sampling is the surgical (VATS) thoracoscopy, allowing direct visual guiding of tissue sampling from all pleural surfaces. Yet, globally the medical (pleuroscopy) thoracoscopy is more widely used: cheaper, outpatient procedure, but allows only sampling from the parietal pleura. To date, no randomised studies have compared medical and surgical thoracoscopy concerning diagnostic hit rates, adverse events, or economics.
Investigators will perform two randomized studies to investigate whether
PET/CT is comparable to CT alone
VATS is comparable to pleuroscopy concerning hit rate, total investigations performed, time-to-diagnosis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Neoplasms
Keywords
Thoracoscopy
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Pleuroscopy
Arm Type
Active Comparator
Arm Description
According to BTS guideline thoracoscopy is the next procedure for patients who remain undiagnosed despite PET-CT and attempts to obtain biopsies. Eligible patients will be randomised to pleuroscopy or VATS. Patients with inconclusive pleuroscopy will proceed to VATS.
Arm Title
VATS (thoracoscopy)
Arm Type
Active Comparator
Arm Description
According to BTS guideline thoracoscopy is the next procedure for patients who remain undiagnosed despite PET-CT and attempts to obtain biopsies. Eligible patients will be randomised to pleuroscopy or VATS. Patients with inconclusive pleuroscopy will proceed to VATS.
Intervention Type
Device
Intervention Name(s)
Thoracoscopy
Intervention Description
50 % of patients will have performed af medical thoracoscopy (pleuroscopy)
Intervention Type
Device
Intervention Name(s)
VATS (thoracoscopy)
Intervention Description
50 % of patients will have performed a VATS (video-assisted thoracic surgery) thoracoscopy
Primary Outcome Measure Information:
Title
Number of patients diagnosed with cancer
Description
(cancer = an unequivocal diagnosis of neoplastic disease; no cancer = clinically benign cause, and improved imaging at 6 month control).
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Quality of life
Description
Questionnaire developed to assess the quality of life of cancer patients, QLQC 30
Time Frame
1 month
Title
Total costs
Description
calculated as costs patient-related, procedure-related, and overall
Time Frame
2 years
Title
Pain
Description
VAS scale
Time Frame
2 years
Title
Quality of life
Description
A standardised instrument for use as a measure of health outcome, EuroQol EQ-5D
Time Frame
1 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with recurrent pleural effusion of unknown origin after a first pleural tap according to BTS guidelines.
Indication for thoracoscopy according to BTS guidelines.
Patients accept further investigation according to Danish and BTS guidelines.
Have received oral and written consent and agreed.
At the time of inclusion, above 18 years of age.
Exclusion Criteria:
Female patients: pregnancy or breastfeeding.
Lack of language comprehension.
Legally incompetent patients.
Life expectancy less than 3 month.
Contraindications to pleural tissue sampling.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Uffe Boedtger, MD, PhD
Organizational Affiliation
Syddansk Universitet
Official's Role
Study Director
Facility Information:
Facility Name
Naestved Hospital
City
Naestved
ZIP/Postal Code
4700
Country
Denmark
12. IPD Sharing Statement
Learn more about this trial
Rational Approach to a Unilateral Pleural Effusion
We'll reach out to this number within 24 hrs