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Pneumothorax clinical trials

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NCT ID: NCT00563641 Completed - Clinical trials for Respiratory Distress Syndrome

Very Early Surfactant and NCPAP for Premature Infants With RDS

CNRNCPAP
Start date: January 2004
Phase: Phase 3
Study type: Interventional

The present study will test the use of very early nasal continuous airway pressure(NCPAP)with and without surfactant in premature infants with clinical evidence or respiratory distress syndrome. We hypothesize that premature infants exposed to very early NCPAP and surfactant will require less mechanical ventilation compared to those premature infants exposed to NCPAP alone.

NCT ID: NCT00562302 Completed - Pneumothorax Clinical Trials

Bio-Seal Biopsy Track Plug for Reducing Pneumothorax Rates Post Lung Biopsy Procedure

Start date: April 2005
Phase: Phase 3
Study type: Interventional

BS-1053 A Prospective Randomized Multi-Centered Safety and Efficacy Evaluation of the Bio-Seal Biopsy Track Plug for Reducing Pneumothorax Rates Post Lung Biopsy Procedures

NCT ID: NCT00556335 Completed - Pneumothorax Clinical Trials

Pneumothorax Therapy: Manual Aspiration Versus Conventional Chest Tube Drainage

pneumothorax
Start date: April 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy of manual aspiration in comparison to conventional chest tube drainage in pneumothorax therapy: 1. whether manual aspiration will shorten hospital admission. 2. whether the lung will expand by means of clinical and radiological findings.

NCT ID: NCT00544479 Completed - Pneumothorax Clinical Trials

No Routine CXR After Bronchoscopy

Start date: March 2015
Phase:
Study type: Observational

Most pulmonologist request a routine chest-x-ray after bronchoscopy with transbronchial biopasie to exclude pneumothorax. We published a study in CHEST showing that routine chest-ray might not be necessary. We would like to conduct a propsective study to validate the results of the CHEST-study. Before and after the procedure follwing information will be collected: Age, Sex, Indication for procedure, number of biopsies and segment of biopsie, Saturation, Physical examination, Symptoms suggestive of pneumothorax. If there is no aggravation of the symptoms and/or physical examination after the procedure, as compared to before, routine chest-x-ray will NOT be done. A phone will be made 24 to 48 hours following the procedure to the patient.

NCT ID: NCT00530725 Completed - Pneumothorax Clinical Trials

Management of Occult Pneumothoraces in Mechanically Ventilated Patients

OPTICC
Start date: August 2006
Phase: N/A
Study type: Interventional

Collapsed lungs are common injuries after traumatic injury that regularly cause needless deaths despite being treatable with chest tubes. Properly used these tubes can be life-saving. Unfortunately, improperly used they can cause pain, bleeding, and other fatal complications themselves. Over the last few decades with increased use of CT scanning it is apparent that many small collapsed lungs are not seen on chest X-rays, and there is little guidance for the treating Doctors as to how to treat these patients. There is almost no good data that tells us whether these smaller pneumothoraces require treatment with chest tubes or whether they can simply be closely watched. This proposal is to carry out a simple trial of randomly assigning patients who do not appear to have any symptoms or problems from their occult pneumothorax to either having a standard chest tube or to being watched. Our careful review of the medical literature indicates that the investigators cannot honestly tell patients and their families which treatment is best or required. Our audit of current practice also indicates that Doctors in Calgary and across Canada, regularly prescribe both treatments regularly but in a hap-hazard. The patients in this study will be very closely watched in the intensive care unit and if they develop any breathing problems and do not have a chest tube in, then one will be inserted. The main results that the investigators are trying to determine with this pilot study, though, is whether the investigators are able to detect appropriate patients, to recruit them into such a study, and whether the guidelines the investigators have created to manage these patients in this study will be acceptable to all the patient's care givers. This data will help us to design a future large multi-centre trial that will hopefully provide information as how best to manage this type of injured patient.

NCT ID: NCT00520221 Completed - Pneumothorax Clinical Trials

Intrapleural Minocycline Following Simple Aspiration for Primary Spontaneous Pneumothorax

Start date: January 2004
Phase: N/A
Study type: Observational

The optimal initial management of primary spontaneous pneumothorax (PSP) remains controversial. This study was conducted to evaluate the safety and efficacy of additional minocycline pleurodesis after successful aspiration of the first episode of PSP.

NCT ID: NCT00188409 Completed - Lung Nodules Clinical Trials

Pneumothorax Post CT Lung Biopsy

Start date: February 2002
Phase: N/A
Study type: Interventional

A CT scan is performed after a lung biopsy in order to detect a Pneumothorax. We postulate that CT is more useful than chest radiography