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Clinical Trials/NCT02002273
NCT02002273
Withdrawn
Not Applicable

The Effect of Regulated Pleural Pressure on The Duration of Air Leak and Fluid Drainage Following Pulmonary Anatomic Resections: A Multicenter Randomized Trial

Ospedali Riuniti Ancona1 site in 1 countryJanuary 2014
ConditionsLung Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lung Cancer
Sponsor
Ospedali Riuniti Ancona
Locations
1
Primary Endpoint
duration of air leak
Status
Withdrawn
Last Updated
10 years ago

Overview

Brief Summary

The objective of this randomized study is to compare the effect of two controlled chest tube protocols on the duration of air leak and fluid drainage following pulmonary lobectomy or segmentectomy by using an electronic regulated chest drainage system (Thopaz). Previous studies have suggested that the amount of negative pressure used at the level of the chest drainage device may affect the duration of air leak, but the results have been inconsistent, however as revealed in more recent studies understanding of the physics of chest drainage devices may have been confounded by lack of regulation of the pleural pressure.

In addition, experimental studies have shown that fluid drainage may be affected by the degree of negative pleural pressure applied.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
January 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Ospedali Riuniti Ancona
Responsible Party
Principal Investigator
Principal Investigator

Cecilia Pompili

MD

Ospedali Riuniti Ancona

Eligibility Criteria

Inclusion Criteria

  • Able and willing to read, understand, and provide written Informed Consent;
  • Age range of 18-90 years;
  • Patients submitted to lobectomy, segmentectomy and bilobectomy due to lung cancer or other intrathoracic lesions. Both open and minimally invasive (thoracoscopic) resections are acceptable.

Exclusion Criteria

  • if patients are submitted to lung resection associated with chest wall resection or diaphragm resection the patient will be excluded from analysis
  • If during the postoperative hospital course there is a need for postoperative mechanical ventilation or hemodynamic instability the patient will be excluded from analysis.
  • If the subject meets all of the inclusion criteria and none of the exclusion criteria, he/she is eligible to participate in the study.

Outcomes

Primary Outcomes

duration of air leak

Time Frame: up to 7 days

Secondary Outcomes

  • 1. Differences in airflow detected during the 4 hours after the pressure level is switched to -8 cmH2O or -20 cmH2O compared to the original pressure level in both groups(up to 5 days)
  • Differences in fluid drainage(up to 5 days)
  • Duration of chest tube left in the patient (days)(up to 7 days)
  • Postoperative length of hospital stay (days)(up to 7 days)

Study Sites (1)

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