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Pleural Effusion clinical trials

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NCT ID: NCT02227732 Completed - Clinical trials for Malignant Pleural Effusions

A Pilot Study Evaluating the Safety and Effectiveness of a New Pleural Catheter for the Medical Management of Symptomatic, Recurrent, Malignant Pleural Effusions

Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a new catheter is safe and effective in treating malignant pleural effusions.

NCT ID: NCT02208895 Completed - Pleural Effusions Clinical Trials

iSTAT Comparison Study, IRB3785

Start date: February 2014
Phase:
Study type: Observational

Pleural fluid glucose levels measured with bed-side point of care methods such as finger stick glucometers and I-STAT device correlate with the traditional in-lab testing methods.

NCT ID: NCT02192138 Completed - Pleural Effusion Clinical Trials

Pathophysiological Effects of Intrapleural Pressure Changes During Therapeutic Thoracentesis

Start date: August 2014
Phase: N/A
Study type: Interventional

Research project objectives. The project includes eight research hypotheses and eight corresponding study objectives. The most relevant objectives are: - Analysis of lung function and gas exchange parameters in relation to the removed pleural fluid volume and intrapleural pressure changes. - Evaluation of changes in lung and chest wall compliance and related changes in work of breathing during therapeutic thoracentesis and pleural fluid withdrawal. - Study of the relationship between intrapleural pressure changes and cardiac function assessed by echocardiography and alterations in serum natriuretic peptide A and B concentration. - Comparative analysis of the reliability of the volume-pressure curve slope prediction based on different variables measured before thoracentesis and real measurements of ventilation and intrapleural pressure during thoracentesis. 2. Research methodology The study will be performed in 60 patients with pleural effusion planned for therapeutic thoracentesis. Studies before thoracentesis: body plethysmography, spirometry, lung diffusion capacity (DLCO), arterial blood gases, 6 minute walk test, echocardiography, serum natriuretic peptide concentration. Evaluation during thoracentesis: continuous measurement of tidal breathing and respiratory rate, measurement of removed pleural fluid volume and intrapleural pressure, transcutaneous measurement of PO2 and PCO2. Pleural catheter will be retained for the next 48hours to enable fluid drainage and intrapleural pressure measurement after completion of thoracentesis. Monitoring during 48-hrs after thoracentesis: pre-thoracentesis measurements will be repeated in specific time points and compared in two subgroups (active physiotherapy to improve lung re-expansion and passive lung re-expansion). Intrapleural pressure will be measured 24 and 48 hours after thoracentesis. Then, the catheter will be removed. Analysis.Signal analysis and visual multidimensional analysis performed with the use of own computer programs will be the first step of the analysis. The identified relationships between the analyzed parameters should allow to form physiological, medical, and statistical hypotheses, as well to verify the analysis of previously obtained data . Expected impact of the research project The study results will allow to define lung function, blood gases and cardiovascular function in relation to changes in intrapleural pressure. Some of these correlations had not been previously investigated. Our results may influence management standards in patients who require therapeutic thoracentesis.

NCT ID: NCT02191540 Completed - Clinical trials for Malignant Pleural Effusion

Efficacy and Safety Study of Abnoba Viscum F 20mg in Malignant Pleural Effusion Patients

Start date: January 2011
Phase: Phase 3
Study type: Interventional

Phase 3, non-randomized, Multicenter, single arm study to assess efficacy and safety of Abnoba viscum F 20mg in patients with malignant pleural effusion

NCT ID: NCT02147821 Completed - Clinical trials for Pleural Effusions Post Coronary Artery Bypass Graft

Necessity of Using Pleural Drainage Tubes After IMA Harvesting During Cardiac Surgery

Start date: August 2014
Phase: N/A
Study type: Interventional

This prospective randomized controlled trial will examine the efficacy of reducing the number of chest tubes used in the postoperative cardiac surgery patient. Typically used are three chest tubes - two in the mediastinum and one in the pleural space, if opened. The investigators propose that removal of the pleural tube will not impact the rates of clinically significant pleural effusions post cardiac surgery. Patients will be randomized into two groups - one receiving the standard three chest tubes (standard), and the other receiving only mediastinal drains (experimental). The primary outcome will be rates of post-operative pleural effusions as determined by defined interventions, including insertion of a chest tube, thoracentesis, or return to the operating room for primary evacuation of pleural effusion or hemothorax. Secondary outcomes include length of hospital stay, length of mechanical ventilation, postoperative respiratory status, and presence/size of pleural effusions, as well as readmission for pleural effusion.

NCT ID: NCT02054052 Completed - Clinical trials for Non-small Cell Lung Cancer

Intrapleural Bevacizumab Injection for Malignant Effusion in Lung Cancer

Start date: January 2014
Phase: Phase 2
Study type: Interventional

Malignant pleural or pericardial effusion is common in lung cancer, and intrapleural drugs injection is important in the treatment. Non- cytotoxic drugs include those with a sclerosing effect that produces pleurodesis, which is easy to cause severe chest pain despite of no influence on the following chemotherapy. Tumor angiogenesis is important in producing MPE. Bevacizumab has been administrated locally in treating optic nerve sickness successfully by anti-VEGF mechanism. So we hypothesize that intrapleural bevacizumab is also effective in treating MPE.

NCT ID: NCT02045641 Completed - Heart Disease Clinical Trials

Pleural and Pericardial Effusion Following Open Heart Surgery

IMAGING
Start date: September 2013
Phase: N/A
Study type: Interventional

One of the most common postoperative complications after open cardiac surgery is fluid accumulation between the pleural membranes or in the pericardial sac. This study investigates the consequence of such fluid accumulations on physical performance, recovery-time, cardiac and respiratory complications, and quality of life. Half of the participants will be followed closely and offered fluid drainage at a low threshold, and half of the participants will follow the current postoperative regimen.

NCT ID: NCT02036398 Completed - Pleural Effusion Clinical Trials

Tubeless Versus Standard Upper Pole Percutaneous Nephrolithotomy

Start date: January 2013
Phase: N/A
Study type: Interventional

Comparison of complications between standard upper pole percutaneous nephrolithotomy (PCNL) with nephrostomy placement and double J stent and PCNL with double J placement only without nephrostomy.

NCT ID: NCT01997190 Completed - Breast Cancer Clinical Trials

Intrapleural AdV-tk Therapy in Patients With Malignant Pleural Effusion

MpeTK01
Start date: October 2013
Phase: Phase 1
Study type: Interventional

This is a phase I study of intrapleural AdV-tk therapy in patients with malignant pleural effusion (MPE). The primary objective is to test the safety of intrapleural AdV-tk therapy. Secondary objectives are to evaluate clinical efficacy and biologic activity

NCT ID: NCT01994499 Completed - Clinical trials for Infectious Pleural Effusion

Randomized Study Comparing Pleural Drainage by Videothoracoscopy to Medical Drainage in Infectious Pleural Effusion

VIDMED
Start date: January 24, 2014
Phase: N/A
Study type: Interventional

Infectious pleural effusion is a classic complication of pneumonia and often require pleural drainage. There is no consensus between surgical drainage and medical drainage indication in first intention to treat an empyema. Usually surgery is proposed in second intention after failure of medical drainage. Videothoracoscopy is well accepted in diagnosis and treatment of pleural pathologies. The morbidity of this approach is very low with good results and become the gold standard in different pleural diseases. The medical drainage can be also very efficient but its results depends of the evolution of the pleural effusion. The rate of failure is estimated around 25%. Then, the aim of our study is to compare surgical drainage and medical drainage in first intention. The first end-point will be the hospital stay (day). Hospital discharge will be strict, following different objective criteria of healing allowing comparison between these two approaches of drainage. To answer this question we will randomized 50 patients in 2 years with a multicenter recruitment.