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MesoTRAP: A Study Comparing Video-assisted Thoracoscopic Partial Pleurectomy/Decortication With Indwelling Pleural Catheter in Patients With Trapped Lung Due to Malignant Pleural Mesothelioma. (MesoTRAP)

Primary Purpose

Malignant Pleural Mesothelioma, Trapped Lung

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
pleurectomy/decortication
indwelling pleural catheter
Sponsored by
Papworth Hospital NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malignant Pleural Mesothelioma focused on measuring pleurectomy/decortication, indwelling pleural catheter

Eligibility Criteria

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

Inclusion Criteria:

  1. Pathologically confirmed MPM
  2. Trapped lung, defined as a 'clinically significant trapped lung requiring intervention in the opinion of the clinical team"
  3. Pleural effusion present (following re-accumulation)
  4. Considered by the clinical team to be suitable and fit enough to undergo VAT-PD
  5. Community services or patient/carer able to drain IPC at least twice weekly
  6. Considered by the clinical team to be equally suitable for treatment with VAT-PD or IPC, and therefore eligible for treatment allocation by randomisation.
  7. Patient willing to receive either VAT-PD or IPC and attend the respective designated centre for their treatment
  8. Expected survival of at least 4 months, as assessed by managing clinician
  9. Age ≥ 18 years
  10. Able to provide informed consent

Exclusion Criteria:

  1. Lung re-expands fully following pleural fluid drainage i.e. no entrapment
  2. Evidence of active pleural infection
  3. Current participation in an RCT or CTIMP
  4. Females: pregnant or lactating

Sites / Locations

  • Blackpool Teaching Hospitals NHS Foundation Trust
  • North Bristol NHS Trust
  • Papworth Hospital NHS Foundation Trust
  • Cambridge University Hospitals
  • Derby Teaching Hospitals NHS Foundation Trust
  • Golden Jubilee National Hospital
  • Queen Elizabeth University Hospital and New Victoria Hospital
  • University Hospitals of Leicester
  • Barts Health NHS Trust
  • Manchester University NHS Foundation Trust
  • Pennine Acute Hospitals NHS Trust
  • Norfolk and Norwich University Hospitals NHS Foundation Trust
  • Nottingham University Hospitals NHS Trust
  • Oxford University Hospitals
  • North West Anglia NHS Foundation Trust
  • Lancashire Teaching Hospitals NHS Foundation Trust
  • Sheffield Teaching Hospitals
  • University Hospitals of North Midlands NHS Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

pleurectomy/decortication

indwelling pleural catheter

Arm Description

Outcomes

Primary Outcome Measures

To measure the standard deviation of Visual Analogue Scale scores for breathlessness
The Visual Analogue Scale (VAS) is a 100mm line for patients to record the severity of a their breathlessness where 0mm is "No breathlessness at all" and 100mm is "Worst possible breathlessness".

Secondary Outcome Measures

To measure the standard deviation of Visual Analogue Scale scores for chest pain
The Visual Analogue Scale (VAS) is a 100mm line for patients to record the severity of a their chest pain where 0mm is "No pain at all" and 100mm is "Worst possible pain".
Quality of Life measured using the EQ-5D-5L
Quality of Life measured using the EORTC QLQC30
Survival at 30 days and 12 months post randomisation
Adverse events
The prevalence of trapped lung in patients with MPM
Percentage of eligible patients in participating centres
Recruitment rate
To assess completion of resource use data during follow-up using patients' routine data

Full Information

First Posted
November 29, 2017
Last Updated
September 15, 2020
Sponsor
Papworth Hospital NHS Foundation Trust
Collaborators
National Institute for Health Research, United Kingdom, London School of Hygiene and Tropical Medicine, King's College London, University of Sheffield
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1. Study Identification

Unique Protocol Identification Number
NCT03412357
Brief Title
MesoTRAP: A Study Comparing Video-assisted Thoracoscopic Partial Pleurectomy/Decortication With Indwelling Pleural Catheter in Patients With Trapped Lung Due to Malignant Pleural Mesothelioma.
Acronym
MesoTRAP
Official Title
MesoTRAP: A Pilot Clinical Trial and Feasibility Study Comparing Video-assisted Thoracoscopic Partial Pleurectomy/Decortication With Indwelling Pleural Catheter in Patients With Trapped Lung Due to Malignant Pleural Mesothelioma Designed to Address Recruitment and Randomisation Uncertainties and Sample Size Requirements for a Phase III Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
August 10, 2017 (Actual)
Primary Completion Date
March 31, 2020 (Actual)
Study Completion Date
August 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Papworth Hospital NHS Foundation Trust
Collaborators
National Institute for Health Research, United Kingdom, London School of Hygiene and Tropical Medicine, King's College London, University of Sheffield

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
Malignant pleural mesothelioma is a cancer, caused by asbestos, which currently affects 2500 people in the UK each year. The main symptom is breathlessness caused by fluid building up in the space between the lung and the chest wall (pleural effusion). Treatment involves draining the fluid to allow the lung to re-expand (pleurodesis). However, sometimes tumour growth over the surface of the lung can prevent it from re-expanding. This 'trapped' lung results in fluid re-accumulation and repeated drainage which can lead to discomfort and multiple hospital visits. One approach to dealing with 'trapped' lung in mesothelioma is to insert a thin tube (Indwelling Pleural Catheter - IPC) into the space around the lung. The tube can stay in place for a long time allowing patients to drain off fluid at home. Another approach is a keyhole surgical operation (video-assisted thoracoscopic partial pleurectomy/decortication - VAT-PD) to remove as much tumour as possible from the lining of the lung to allow it to re-expand. While both approaches are currently offered in clinical practice, it is not known which of the two is most effective at relieving breathlessness. The only way to find out is to conduct a research trial comparing the two. The Investigators plan to do this, but first of all need to carry out a small pilot study to collect information necessary to help plan the full study.
Detailed Description
This is a multi-centre, open-label, randomised controlled pilot clinical trial and feasibility study comparing video-assisted thoracoscopic partial pleurectomy/decortication (VAT-PD) with indwelling pleural catheter (IPC) in patients with trapped lung (TL) and pleural effusion due to malignant pleural mesothelioma (MPM), aimed at addressing recruitment and randomisation uncertainties as well as sample size requirements for a full phase III study. 38 patients will be randomised and allocated in a 1:1 ratio to either VAT-PD or IPC. The study will be undertaken at mesothelioma surgical centres with expertise in either IPC, VAT-PD or both procedures, together with their linked non-surgical referral hospitals (hub and spoke). Patients meeting all eligibility criteria will be informed about the study, provided with a patient information sheet and given at least 24 hours to consider participation. Following consent, patients will be randomised, baseline measurements will be taken and a procedure date will be arranged. Following the procedure follow-up visits at 6 weeks, 3, 6 and 12 months post-randomisation are planned to coincide with clinical care visits. In parallel with the main study an observational sub-study will collect observational data on a cohort of patients who have Malignant Pleural Mesothelioma and trapped lung, but who are either not eligible to participate, or who decline to participate in the main study. Patients in the Observational Sub-study will receive the same baseline and follow-up visits as those in the main study, but will receive standard clinical care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malignant Pleural Mesothelioma, Trapped Lung
Keywords
pleurectomy/decortication, indwelling pleural catheter

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
pleurectomy/decortication
Arm Type
Experimental
Arm Title
indwelling pleural catheter
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
pleurectomy/decortication
Other Intervention Name(s)
video-assisted thoracoscopic partial pleurectomy/decortication, VAT-PD
Intervention Description
VAT-PD is a type of "keyhole surgery" performed under general anaesthesia using a telescope and instruments put inside the chest. Through small incisions, or keyholes made between the ribs, the thoracic surgeon removes the hard rind of the tumour over the surface of the lung, thereby allowing the 'trapped' lung to fully expand again. Simultaneous removal of mesothelioma from the outer pleural membrane allows pleurodesis to occur.
Intervention Type
Procedure
Intervention Name(s)
indwelling pleural catheter
Other Intervention Name(s)
IPC
Intervention Description
A soft silicone catheter (IPC) with a one-way valve at the end is inserted a few centimetres under the skin under local anaesthesia. The inside end of the catheter is inserted into the pleural space and the outside end is connected to a vacuum drainage bottle. The IPC permits regular fluid drainage.
Primary Outcome Measure Information:
Title
To measure the standard deviation of Visual Analogue Scale scores for breathlessness
Description
The Visual Analogue Scale (VAS) is a 100mm line for patients to record the severity of a their breathlessness where 0mm is "No breathlessness at all" and 100mm is "Worst possible breathlessness".
Time Frame
Daily from randomisation to 12 months
Secondary Outcome Measure Information:
Title
To measure the standard deviation of Visual Analogue Scale scores for chest pain
Description
The Visual Analogue Scale (VAS) is a 100mm line for patients to record the severity of a their chest pain where 0mm is "No pain at all" and 100mm is "Worst possible pain".
Time Frame
Daily from randomisation to 12 months
Title
Quality of Life measured using the EQ-5D-5L
Time Frame
Baseline, intervention, 6 weeks, 3, 6 and 12 months post randomisation
Title
Quality of Life measured using the EORTC QLQC30
Time Frame
Baseline, intervention, 6 weeks, 3, 6 and 12 months post randomisation
Title
Survival at 30 days and 12 months post randomisation
Time Frame
30 days and 12 months post randomisation
Title
Adverse events
Time Frame
From randomisation to the end of study follow-up (expected to be 12 months)
Title
The prevalence of trapped lung in patients with MPM
Time Frame
From beginning to end of recruitment period (18 months)
Title
Percentage of eligible patients in participating centres
Time Frame
From beginning to end of recruitment period (18 months)
Title
Recruitment rate
Time Frame
From beginning to end of recruitment period (18 months)
Title
To assess completion of resource use data during follow-up using patients' routine data
Time Frame
Baseline, intervention, 6 weeks, 3, 6 and 12 months post randomisation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pathologically confirmed MPM Trapped lung, defined as a 'clinically significant trapped lung requiring intervention in the opinion of the clinical team" Pleural effusion present (following re-accumulation) Considered by the clinical team to be suitable and fit enough to undergo VAT-PD Community services or patient/carer able to drain IPC at least twice weekly Considered by the clinical team to be equally suitable for treatment with VAT-PD or IPC, and therefore eligible for treatment allocation by randomisation. Patient willing to receive either VAT-PD or IPC and attend the respective designated centre for their treatment Expected survival of at least 4 months, as assessed by managing clinician Age ≥ 18 years Able to provide informed consent Exclusion Criteria: Lung re-expands fully following pleural fluid drainage i.e. no entrapment Evidence of active pleural infection Current participation in an RCT or CTIMP Females: pregnant or lactating
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Rintoul, Dr
Organizational Affiliation
Papworth Hospital NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Blackpool Teaching Hospitals NHS Foundation Trust
City
Blackpool
Country
United Kingdom
Facility Name
North Bristol NHS Trust
City
Bristol
Country
United Kingdom
Facility Name
Papworth Hospital NHS Foundation Trust
City
Cambridge
ZIP/Postal Code
CB23 5EF
Country
United Kingdom
Facility Name
Cambridge University Hospitals
City
Cambridge
Country
United Kingdom
Facility Name
Derby Teaching Hospitals NHS Foundation Trust
City
Derby
Country
United Kingdom
Facility Name
Golden Jubilee National Hospital
City
Glasgow
Country
United Kingdom
Facility Name
Queen Elizabeth University Hospital and New Victoria Hospital
City
Glasgow
Country
United Kingdom
Facility Name
University Hospitals of Leicester
City
Leicester
Country
United Kingdom
Facility Name
Barts Health NHS Trust
City
London
Country
United Kingdom
Facility Name
Manchester University NHS Foundation Trust
City
Manchester
Country
United Kingdom
Facility Name
Pennine Acute Hospitals NHS Trust
City
Manchester
Country
United Kingdom
Facility Name
Norfolk and Norwich University Hospitals NHS Foundation Trust
City
Norwich
Country
United Kingdom
Facility Name
Nottingham University Hospitals NHS Trust
City
Nottingham
Country
United Kingdom
Facility Name
Oxford University Hospitals
City
Oxford
Country
United Kingdom
Facility Name
North West Anglia NHS Foundation Trust
City
Peterborough
Country
United Kingdom
Facility Name
Lancashire Teaching Hospitals NHS Foundation Trust
City
Preston
Country
United Kingdom
Facility Name
Sheffield Teaching Hospitals
City
Sheffield
Country
United Kingdom
Facility Name
University Hospitals of North Midlands NHS Trust
City
Stoke-on-Trent
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
30687504
Citation
Matthews C, Freeman C, Sharples LD, Fox-Rushby J, Tod A, Maskell NA, Edwards JG, Coonar AS, Sivasothy P, Hughes V, Rahman NM, Waller DA, Rintoul RC. MesoTRAP: a feasibility study that includes a pilot clinical trial comparing video-assisted thoracoscopic partial pleurectomy decortication with indwelling pleural catheter in patients with trapped lung due to malignant pleural mesothelioma designed to address recruitment and randomisation uncertainties and sample size requirements for a phase III trial. BMJ Open Respir Res. 2019 Jan 5;6(1):e000368. doi: 10.1136/bmjresp-2018-000368. eCollection 2019.
Results Reference
derived

Learn more about this trial

MesoTRAP: A Study Comparing Video-assisted Thoracoscopic Partial Pleurectomy/Decortication With Indwelling Pleural Catheter in Patients With Trapped Lung Due to Malignant Pleural Mesothelioma.

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