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Pneumothorax Therapy: Manual Aspiration Versus Conventional Chest Tube Drainage (pneumothorax)

Primary Purpose

Pneumothorax

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
manual aspiration
conventional drainage
Sponsored by
Isala
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pneumothorax focused on measuring manual aspiration, conventional, length of stay

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients with a first episode of a symptomatic pneumothorax admitted to the ER of the hospital (spontaneous or traumatic) or
  • patients with an asymptomatic pneumothorax with a size of ≥ 20 % as estimated by Light's formula
  • age ≥ 18 and < 85 years
  • smoking is tolerated

Exclusion Criteria:

  • recurrent pneumothorax
  • lung fibrosis
  • patients with (lung) cancer
  • pregnant women
  • comorbidity limiting decision making (psychiatric disease, alcohol or drug abuse)
  • prior randomisation
  • Marfan syndrome
  • COPD patients
  • tension pneumothorax
  • multitrauma patients

Sites / Locations

  • Isala Klinieken

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

manual aspiration

conventional drainage

Arm Description

manual aspiration

conventional drainage

Outcomes

Primary Outcome Measures

The duration of length of stay of each technique

Secondary Outcome Measures

The success rate of each technique

Full Information

First Posted
November 9, 2007
Last Updated
April 5, 2013
Sponsor
Isala
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1. Study Identification

Unique Protocol Identification Number
NCT00556335
Brief Title
Pneumothorax Therapy: Manual Aspiration Versus Conventional Chest Tube Drainage
Acronym
pneumothorax
Official Title
A Prospective, Randomised Trial in Pneumothorax Therapy: Manual Aspiration Versus Conventional Chest Tube Drainage
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Completed
Study Start Date
April 2007 (undefined)
Primary Completion Date
April 2010 (Actual)
Study Completion Date
April 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Isala

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the efficacy of manual aspiration in comparison to conventional chest tube drainage in pneumothorax therapy: whether manual aspiration will shorten hospital admission. whether the lung will expand by means of clinical and radiological findings.
Detailed Description
No consensus has been defined concerning the exact treatment of a first episode of SP. Literature suggests similar immediate and long-term efficacy of manual aspiration and chest tube drainage. Morbidity of manual aspiration is low and the procedure is well tolerated. Manual aspiration is safe with a complication rate of only 1 % and can be performed in the outpatient clinic in the majority of patients reducing costs. Our aim is to re - evaluate these findings with a mono-centre study with 114 patients, set-up for the first time in the Netherlands with an expectancy to confirm the former findings. Aim of the study: To evaluate the efficacy of manual aspiration in comparison to conventional chest tube drainage in pneumothorax therapy: whether manual aspiration will shorten hospital admission. whether the lung will expand by means of clinical and radiological findings. Study design: prospective single-centre, open randomised trial. Randomisation: With a computer minimization program for manual aspiration or usual care with special attendance to the cause of pneumothorax (spontaneous or traumatic), the presence of smoking and gender. Statistical analysis: Our primary aim is to demonstrate a higher efficacy for manual aspiration in terms of a shorter admission duration (LOS) in favor of manual aspiration with similar therapy success rates. We will analyse data on an intention to treat basis. P-values below 5 % will be considered statistically significant. Normal distribution will be checked. Means (standard deviations) or medians (ranges or interquartile ranges) will be calculated and unpaired t-tests or Mann Whitney U tests will be used as appropriate to test differences in LOS. Categorical data (success rates) will be analysed using Chi2-tests. Data analysis will be performed using SPSS version 12. Study population: Patients with the first episode of a symptomatic pneumothorax or an asymptomatic pneumothorax with a size ≥ 20 % as estimated by Light's formula ( (1-L/H )x100 ) with an age of ≥ 18 and < 85 years. Intervention: Manual aspiration or conventional chest tube drainage. Primary study endpoint 1. The LOS. Secondary endpoint: 1.The success rate of each technique: Conventional chest tube drainage; complete expansion of the lung, counteraction of the air leak and removal of the drain within 72 hours. Manual aspiration: complete expansion and discharge within 24 hours, success rate at two weeks (continuous expansion) and one year (no recurrence of pneumothorax in the interval period after discharge between 2 weeks and 1 year). Burden, risks and advantages associated with participation: The risks of manual aspiration and chest tube drainage techniques are the same. Complications seem to be occur in only 1 % of the aspirations and they consist of haematothorax, retained catheter tips, subcutaneous emphysema and vasovagal reactions. The most important disadvantage is in case of an unsuccessful treatment by manual aspiration with a persisting pneumothorax. Patients in this case have to undergo the conventional tube chest drainage after all. The benefit of the investigational approach is that patients are discharged earlier from the hospital in case of success and its cost effectiveness.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pneumothorax
Keywords
manual aspiration, conventional, length of stay

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
manual aspiration
Arm Type
Experimental
Arm Description
manual aspiration
Arm Title
conventional drainage
Arm Type
Active Comparator
Arm Description
conventional drainage
Intervention Type
Procedure
Intervention Name(s)
manual aspiration
Intervention Description
air aspiration
Intervention Type
Procedure
Intervention Name(s)
conventional drainage
Intervention Description
drainage, pneumocath
Primary Outcome Measure Information:
Title
The duration of length of stay of each technique
Time Frame
1 year
Secondary Outcome Measure Information:
Title
The success rate of each technique
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with a first episode of a symptomatic pneumothorax admitted to the ER of the hospital (spontaneous or traumatic) or patients with an asymptomatic pneumothorax with a size of ≥ 20 % as estimated by Light's formula age ≥ 18 and < 85 years smoking is tolerated Exclusion Criteria: recurrent pneumothorax lung fibrosis patients with (lung) cancer pregnant women comorbidity limiting decision making (psychiatric disease, alcohol or drug abuse) prior randomisation Marfan syndrome COPD patients tension pneumothorax multitrauma patients
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
J.W. van den Berg, Dr.
Organizational Affiliation
Isala Klinieken department of pulmonology
Official's Role
Study Director
Facility Information:
Facility Name
Isala Klinieken
City
Zwolle
ZIP/Postal Code
8011 JW
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
11991872
Citation
Noppen M, Alexander P, Driesen P, Slabbynck H, Verstraeten A. Manual aspiration versus chest tube drainage in first episodes of primary spontaneous pneumothorax: a multicenter, prospective, randomized pilot study. Am J Respir Crit Care Med. 2002 May 1;165(9):1240-4. doi: 10.1164/rccm.200111-078OC.
Results Reference
background
PubMed Identifier
22925840
Citation
Parlak M, Uil SM, van den Berg JW. A prospective, randomised trial of pneumothorax therapy: manual aspiration versus conventional chest tube drainage. Respir Med. 2012 Nov;106(11):1600-5. doi: 10.1016/j.rmed.2012.08.005. Epub 2012 Aug 24.
Results Reference
derived

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Pneumothorax Therapy: Manual Aspiration Versus Conventional Chest Tube Drainage

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