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Minirigid Versus Conventional Rigid Thoracoscopy in Undiagnosed Pleural Effusions (MICRO)

Primary Purpose

Pleural Effusion

Status
Recruiting
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Mini-thoracoscopy
Conventional rigid thoraoscopy
Sponsored by
Postgraduate Institute of Medical Education and Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Pleural Effusion focused on measuring thoracoscopy, pleuroscopy, metastatic cancer, lung cancer, malignant pleural effusion, tuberculosis

Eligibility Criteria

15 Years - 80 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Medical thoracoscopy being performed for obtaining a pleural biopsy

Exclusion Criteria:

  • PaO2/FIO2< 300; Hemodynamic instability Myocardial infarction or unstable angina in the last 6 wk Lack of pleural space due to adhesions Uncorrected coagulopathy Failure to provide informed consent

Sites / Locations

  • Postgraduate Institute of Medical Education and ResearchRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Mini-thoraoscopy

Conventional rigid thoracoscopy

Arm Description

The mini-thoracoscope manufactured by Richard Wolf GmbH, Knettligen, Germany will be used for performing thoracoscopic pleural biopsies. It has an outer diameter of 5.5 mm and a working channel diameter of 3.5 mm.

The rigid thoracoscope manufactured by Richard Wolf GmbH, Knettligen, Germany will be used for performing thoracoscopic pleural biopsies. It has an outer diameter of 10 mm and channel internal diameter of 5 mm.

Outcomes

Primary Outcome Measures

Diagnostic sensitivity (intention-to-treat)
Difference between the diagnostic sensitivity of mini-thoracoscopy and conventional rigid thoracoscopy in the diagnosis of exudative pleural effusions by calculating the number of true positives diagnosed by thoracoscopic biopsy in the two groups out of the total diseased
Diagnostic sensitivity (per protocol)
Diagnostic sensitivity of mini-thoracoscopy and conventional rigid thoracoscopy in the diagnosis of exudative pleural effusions by calculating the number of true positives diagnosed by thoracocopic biopsy. In this analysis, the subjects crossed over to the rigid group (due to failure of minirigid to yield biopsy tissue) will be considered in the rigid group

Secondary Outcome Measures

Sedative and analgesic dose
Comparing doses of sedative and analgesic agents required in the two groups
Pain scores by visual analog scale
Difference between intraoperative pain score associated with the use of the two devices (assessed after the procedure using the visual analog scale from 0-no pain to 100-maximum possible pain) in the two groups
Diagnostic specificity
Difference between the diagnostic specificity of mini-thoracoscopy and conventional rigid thoracoscopy in the diagnosis of exudative pleural effusions by calculating the number of true negatives diagnosed by thoracoscopic biopsy in the two groups out of those not diseased
Adverse effects
Differences between number of participants with treatment-related adverse events as assessed by CTCAE v4.0 in the two groups
Scope maneuverability
Differences between maneuverability of the two thoracoscopes on a visual analog scale (0-100 mm) assessed by the operator
Ease of obtaining biopsy
Differences between ease of obtaining pleural biopsy with the two thoracoscopes on a visual analog scale (0-100 mm) assessed by the operator
Incision size
Difference in the size of the incision required with the use of the two devices
Procedure duration
Difference in the duration of procedure in the two groups
Pain scores by Wong Baker FACES pain rating scale
Difference between intraoperative pain score associated with the use of the two devices (assessed after the procedure using the Wong Baker FACES pain rating scale) in the two groups

Full Information

First Posted
February 17, 2018
Last Updated
March 28, 2023
Sponsor
Postgraduate Institute of Medical Education and Research
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1. Study Identification

Unique Protocol Identification Number
NCT03449602
Brief Title
Minirigid Versus Conventional Rigid Thoracoscopy in Undiagnosed Pleural Effusions
Acronym
MICRO
Official Title
A Randomized Trial Comparing the Diagnostic Sensitivity and Safety of Mini-thoracoscopy Versus Conventional Rigid Thoracoscopy in Undiagnosed Pleural Effusions
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2018 (Actual)
Primary Completion Date
September 30, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Postgraduate Institute of Medical Education and Research

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Consecutive patients who are planned to undergo a medical thoracoscopy for obtaining pleural biopsies will be enrolled in the study. One hundred subjects will be randomized in 1:1 ratio to undergo thoracoscopy to the following groups: Group A (mini-thoracoscopy) Group B (Conventional rigid thoracoscopy) Primary outcome: (a) diagnostic sensitivity of mini-thoracoscopy and conventional rigid thoracoscopy in the diagnosis of exudative pleural effusions
Detailed Description
A significant proportion of patients with pleural effusions remain undiagnosed after performance of diagnostic procedures including cytological and microbiologic analysis of the pleural fluid and closed pleural biopsies. In this study, the investigators plan to compare the yield and safety of mini-thoracoscopy and conventional rigid thoracoscopy with the larger diameter scope. This is a prospective study that will be conducted at the Thoracic Endoscopy Suite of the Department of Pulmonary Medicine, PGIMER, Chandigarh. Consecutive patients who are planned to undergo a medical thoracoscopy for obtaining pleural biopsies will be enrolled in the study One hundred subjects will be randomized in 1:1 ratio to undergo thoracoscopy. The randomization sequence will be generated using a computer (in blocks of 10), and the allocation will be placed in opaque sealed envelopes. The patients will be randomized to the following groups: Group A (mini-thoracoscopy): The mini-thoracoscope manufactured by Richard Wolf GmbH, Knettligen, Germany will be used. It has an outer diameter of 5.5 mm and a working channel diameter of 3.5 mm. Group B (Conventional rigid thoracoscopy): The rigid thoracoscope manufactured by Richard Wolf GmbH, Knettligen, Germany will be used that has an outer diameter of 10 mm and channel internal diameter of 5 mm. Primary outcome: (a) diagnostic sensitivity of mini-thoracoscopy and conventional rigid thoracoscopy in the diagnosis of exudative pleural effusions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pleural Effusion
Keywords
thoracoscopy, pleuroscopy, metastatic cancer, lung cancer, malignant pleural effusion, tuberculosis

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Mini-thoraoscopy
Arm Type
Experimental
Arm Description
The mini-thoracoscope manufactured by Richard Wolf GmbH, Knettligen, Germany will be used for performing thoracoscopic pleural biopsies. It has an outer diameter of 5.5 mm and a working channel diameter of 3.5 mm.
Arm Title
Conventional rigid thoracoscopy
Arm Type
Active Comparator
Arm Description
The rigid thoracoscope manufactured by Richard Wolf GmbH, Knettligen, Germany will be used for performing thoracoscopic pleural biopsies. It has an outer diameter of 10 mm and channel internal diameter of 5 mm.
Intervention Type
Device
Intervention Name(s)
Mini-thoracoscopy
Intervention Description
Thoracoscopic pleural biopsy with the mini-thoracoscope
Intervention Type
Device
Intervention Name(s)
Conventional rigid thoraoscopy
Intervention Description
Thoracoscopic pleural biopsy with the conventional rigid thoraoscope
Primary Outcome Measure Information:
Title
Diagnostic sensitivity (intention-to-treat)
Description
Difference between the diagnostic sensitivity of mini-thoracoscopy and conventional rigid thoracoscopy in the diagnosis of exudative pleural effusions by calculating the number of true positives diagnosed by thoracoscopic biopsy in the two groups out of the total diseased
Time Frame
6 months
Title
Diagnostic sensitivity (per protocol)
Description
Diagnostic sensitivity of mini-thoracoscopy and conventional rigid thoracoscopy in the diagnosis of exudative pleural effusions by calculating the number of true positives diagnosed by thoracocopic biopsy. In this analysis, the subjects crossed over to the rigid group (due to failure of minirigid to yield biopsy tissue) will be considered in the rigid group
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Sedative and analgesic dose
Description
Comparing doses of sedative and analgesic agents required in the two groups
Time Frame
1 day
Title
Pain scores by visual analog scale
Description
Difference between intraoperative pain score associated with the use of the two devices (assessed after the procedure using the visual analog scale from 0-no pain to 100-maximum possible pain) in the two groups
Time Frame
1 day
Title
Diagnostic specificity
Description
Difference between the diagnostic specificity of mini-thoracoscopy and conventional rigid thoracoscopy in the diagnosis of exudative pleural effusions by calculating the number of true negatives diagnosed by thoracoscopic biopsy in the two groups out of those not diseased
Time Frame
6 months
Title
Adverse effects
Description
Differences between number of participants with treatment-related adverse events as assessed by CTCAE v4.0 in the two groups
Time Frame
1 month
Title
Scope maneuverability
Description
Differences between maneuverability of the two thoracoscopes on a visual analog scale (0-100 mm) assessed by the operator
Time Frame
1 day
Title
Ease of obtaining biopsy
Description
Differences between ease of obtaining pleural biopsy with the two thoracoscopes on a visual analog scale (0-100 mm) assessed by the operator
Time Frame
1 day
Title
Incision size
Description
Difference in the size of the incision required with the use of the two devices
Time Frame
1 day
Title
Procedure duration
Description
Difference in the duration of procedure in the two groups
Time Frame
1 day
Title
Pain scores by Wong Baker FACES pain rating scale
Description
Difference between intraoperative pain score associated with the use of the two devices (assessed after the procedure using the Wong Baker FACES pain rating scale) in the two groups
Time Frame
1 day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Medical thoracoscopy being performed for obtaining a pleural biopsy Exclusion Criteria: PaO2/FIO2< 300; Hemodynamic instability Myocardial infarction or unstable angina in the last 6 wk Lack of pleural space due to adhesions Uncorrected coagulopathy Failure to provide informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sahajal Dhooria, MD, DM
Phone
+919530661388
Email
sahajal@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ritesh Agarwal, MD, DM
Phone
+919478402976
Email
agarwal.ritesh@outlook.in
Facility Information:
Facility Name
Postgraduate Institute of Medical Education and Research
City
Chandigarh
ZIP/Postal Code
160012
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Digambar Behera, MD
Phone
+911722756822
Email
dirlrsi@gmail.com

12. IPD Sharing Statement

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Minirigid Versus Conventional Rigid Thoracoscopy in Undiagnosed Pleural Effusions

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