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Pneumothorax clinical trials

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NCT ID: NCT02959203 Completed - Clinical trials for Pneumothorax Iatrogenic Postprocedural

Comparison of Bedside Ultrasound With Chest X-ray for Confirmation of Central Venous Catheter Position

COMBUX
Start date: June 2016
Phase: N/A
Study type: Observational

Background: Insertion of a central venous catheter (CVC) could lead to a variety of complications. To detect those complications, Chest X-ray (CXR) is still the reference standard. However, there are major limitations in performing CXR's in the critical care setting. Aim/objectives: The objective of this study is to compare the use of bedside ultrasound (US) to conventional CXR in visualization of accuracy and safety of the CVC placement. The aim is to eventually replace X-ray with bedside ultrasound as gold standard for the confirmation of CVC-placement in critically ill patients, thereby reducing radiation exposure and unnecessary delay before CVC use. Methods: The bedside US will be performed by the student or attending physician, who is blinded for CXR findings. After US examination, the attending physician (or student) will fill in a structured form, based on an established protocol. CXR will be performed before or after US examination and assessed by a radiologist. The radiologist will be blinded for the findings of the bedside ultrasound to prevent any biases. Final diagnosis will be determined after examination of the complete medical chart.

NCT ID: NCT02916992 Recruiting - Clinical trials for Spontaneous Pneumothorax

Prevalence of Spontaneous Pneumothorax in BHD

Start date: September 2016
Phase: Phase 1
Study type: Interventional

To assess the prevalence of BHD (Birt-Hogg-Dubé syndrome) among patients with spontaneous pneumothorax. Patients who were treated for primary spontaneous pneumothorax in Rijnstate hospital are to be included. Patients will receive a questionnaire. When given consent, the investigators will invite them for a one-time visit to the out-patient clinic. Patients will be asked for a blood sample to determine pathogenic FLCN (folliculin) mutations and a pulmonary CT scan for evaluation of presence of lung cysts.

NCT ID: NCT02907866 Recruiting - Pneumothorax Clinical Trials

Use of Endobronchial Ultrasound Scope (EBUS) Transducer to Identify Pneumothorax-A Feasibility Study

Start date: September 2016
Phase:
Study type: Observational

Endobronchial ultrasound (EBUS) is a technique that uses ultrasound along with bronchoscope to visualize airway wall and structures adjacent to it. Pneumothorax is a known complication from EBUS procedure. To rule out a Pneumothorax after the procedure, a Chest -X-ray is usually done. Point-of-care sonography has emerged as an invaluable tool in the assessment of patients with both traumatic and non-traumatic dyspnea. Multiple studies involving bedside ultrasound has shown that a pneumothorax can easily be ruled out if pleural sliding sign or B lines are visualized on lung ultrasonography; the accuracy of lung ultrasound in ruling out pneumothorax approach computed tomography and exceed plain radiography. Preforming a lung ultrasound using the EBUS bronchoscope tip as a way to rule out pneumothorax has never been described previously. If this is possible it will obviate the need of getting a Chest -X-ray and decrease the dose of radiation that the patient is exposed to. In this study we will demonstrate that the feasibility of using the transducer of the EBUS Bronchoscope to perform bedside lung ultrasound to rule out pneumothorax.

NCT ID: NCT02866305 Recruiting - Clinical trials for Primary Spontaneous Pneumothorax

Study Designed to Optimize the Treatment of Primary Pneumothorax

TOPP
Start date: March 2009
Phase: Phase 0
Study type: Interventional

Knowledge about incidence, risk factors and genetic predispositions of primary spontaneous pneumothorax in young adults is very limited, and treatment has also been controversial.The Aim of this study is to optimize the treatment, estimate the actual incidence, and identify possible risk factors including genetic predispositions.

NCT ID: NCT02840032 Withdrawn - Pneumothorax Clinical Trials

Determination of Pneumothorax Post Lung Biopsy

Start date: July 2016
Phase:
Study type: Observational

Bedside ultrasonography for detection of pneumothorax after transbronchial lung biopsies in lung transplant patients

NCT ID: NCT02771184 Completed - Pulmonary Fibrosis Clinical Trials

Computerized Lung Sound Analysis

CLSA
Start date: April 2016
Phase: N/A
Study type: Interventional

This clinical trial is conducted within the research project 'Computerized Lung Sound Analysis'. The research goal is the development of a system enabling the automatic classification of lung sounds, which will result in a decision support system for physicians. The objective of this trial is to create a small lung sound corpus, enabling the development of a prototype of the described system. Therefore, investigators record lung sounds with several lung sound transducers distributed on the posterior chest of human test subjects.

NCT ID: NCT02709122 Recruiting - Clinical trials for Tension Pneumothorax

Are EMS Personnel Prepared to Identify and Decompression of Tension Pneumothorax

Start date: February 2016
Phase: N/A
Study type: Interventional

The study aims to determine the level of knowledge and skills to recognize and decompression of tension pneumothorax

NCT ID: NCT02644642 Completed - Pneumothorax Clinical Trials

Utility of Disconnection Technique for One Lung Ventilation

Start date: January 2016
Phase: N/A
Study type: Interventional

Lung isolation technique is useful for lung or heart surgeries for better visualization. Double lumen endobronchial tube and bronchial blocker are available for lung isolation. Adding disconnection technique before lung isolation is helpful to accelerate the lung deflation. However, the utility of disconnection technique has never been evaluated in comparison of double lumen tube and bronchial blocker. Therefore, the utility of disconnection technique in two different lung isolation technique, double lumen tube and bronchial blocker will be evaluated

NCT ID: NCT02619591 Completed - Pneumothorax Clinical Trials

Comparison Of Chest Ultrasound Techniques To Identify Clinically Significant Pneumothorax

Start date: September 2011
Phase: N/A
Study type: Interventional

Patients with chest trauma undergo ultrasound to detect a collapsed lung. Two techniques have been described. A single view for each hemi-thorax, and multiple views for each hemithorax. The investigators are comparing these two techniques in a randomized prospective trial.

NCT ID: NCT02573285 Completed - Clinical trials for Spontaneous Pneumothorax

Spontaneous Pneumothorax in Children

Start date: March 10, 2016
Phase: N/A
Study type: Interventional

The objective of this multi-center, non-randomized, prospective pilot study is to examine the rate of successful primary spontaneous pneumothorax (PSP) resolution using the simple aspiration technique. In this study, eligible subjects diagnosed with PSP at eleven participating large children's hospitals (members of the Midwest Pediatric Surgical Clinical Research Consortium) will be enrolled and offered a choice of management with either the simple aspiration protocol or management according to their surgeon's preference, which may include simple aspiration, chest tube placement, or rarely, an operation.