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Pericardial Effusion clinical trials

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NCT ID: NCT02808897 Completed - Atrial Fibrillation Clinical Trials

Active Clearance of Chest Tubes After Cardiac Surgery: A Prospective Randomized Controlled Study

Start date: November 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effectiveness of the PleuraFlow® Active Tube Clearance (ATC) technology in reducing the rate of postoperative atrial fibrillation (POAF) among post cardiac surgery patients and to evaluate the impact of Active Tube Clearance (ATC) on other complications, such as retained blood syndrome (RBS), a composite endpoint including re-exploration for bleeding or tamponade, and interventions for hemothorax, pericardial or pleural effusion.

NCT ID: NCT02673879 Recruiting - Clinical trials for Pericardial Effusion

IMPI 2 - A Trial of Intrapericardial Alteplase in Large Pericardial Effusion

IMPI-2
Start date: February 2016
Phase: Phase 3
Study type: Interventional

The Second Investigation of the Management of Pericarditis (IMPI-2) Trial will compare the effectiveness and safety of complete percutaneous pericardial drainage facilitated by intrapericardial alteplase (recombinant human tissue-type plasminogen activator) to conventional pericardiocentesis when indicated in 2176 patients with large pericardial effusion due to tuberculous and non-tuberculous pericarditis. An internal pilot study of 218 patients will initially confirm the feasibility of conducting a large-scale multi-centre clinical trial of intrapericardial fibrinolysis in patients with large pericardial effusion, and also provide preliminary safety data, following a dose finding study of intrapericardial alteplase.

NCT ID: NCT02260206 Completed - Clinical trials for Pericardial Effusion

Impact of Colchicine Therapy on Arrhythmia Recurrence After Acute Pericardial Effusion

Start date: July 2014
Phase: Phase 4
Study type: Interventional

The effects colchicine administration for acute pericardial effusion after radiofrequency catheter ablation (RFCA) of atrial fibrillation on the recurrences of arrhythmia.

NCT ID: NCT02132884 Terminated - Clinical trials for Stage IV Non-small Cell Lung Cancer

Genetic Sequencing-Informed Targeted Therapy in Treating Patients With Stage IIIB-IV Non-small Cell Lung Cancer

Start date: March 2015
Phase: N/A
Study type: Interventional

This randomized clinical trial studies how well genetic sequencing-informed targeted therapy works in treating patients with stage IIIB-IV non-small cell lung cancer. Targeted therapy is a type of treatment that uses drugs or other substances to identify and attack specific types of tumor cells that may have less harm to normal cells. Genetic sequencing may help identify these specific types of tumor cells in patients with non-small cell lung cancer.

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: NCT01665495 Recruiting - Clinical trials for Pericardial Effusion

Drainage or Pericardiocentesis (DROP) Alone for Recurrent Non-malignant Pericardial Effusions Requiring Intervention

DROP
Start date: December 2011
Phase: N/A
Study type: Interventional

The DROP study is a prospective, multi center, randomized, open-label trial to test the efficacy and safety of extended catheter pericardial drainage in patients with non-malignant pericardial effusions.

NCT ID: NCT01552187 Active, not recruiting - Atrial Fibrillation Clinical Trials

COlchicine for Prevention of the Post-pericardiotomy Syndrome and Post-operative Atrial Fibrillation (COPPS-2 Trial)

COPPS-2
Start date: March 2012
Phase: Phase 3
Study type: Interventional

This is a multicenter, double-blind, randomized trial to assess the efficacy and safety of colchicine for post-pericardiotomy syndrome prevention, post-operative effusions prevention, and post-operative atrial fibrillation prevention.

NCT ID: NCT01266694 Completed - Clinical trials for Pericardial Effusion

Cochicine Treatment for Post- Operative Pericardial Effusion

POPE2
Start date: April 2011
Phase: Phase 4
Study type: Interventional

Background: The incidence of asymptomatic pericardial effusion is high after cardiac surgery. Objective: To assess whether colchicine is effective in reducing post operative pericardial effusion volume. Design: Multicenter, randomized, double-blind, placebo-controlled study. Intervention : colchicine 1mg vs placebo, once daily for 14 days Setting :10 post operative cardiac rehabilitation centers. Patients: 200 patients at high risk of tamponade because of moderate to large persistent pericardial effusion (grade 2, 3 or 4 on a scale of 0 to 4 measured by echocardiography) more than 7 days after cardiac surgery. Measurements: The main end point will be change in effusion grade after 14 days of treatment. Secondary endpoints include frequency of late cardiac tamponade.

NCT ID: NCT00684125 Completed - Clinical trials for Pericardial Effusion

Evaluation of Different Strategies of Pericardial Drainage After Aortic Valvular Surgery

Blake
Start date: June 2008
Phase: N/A
Study type: Interventional

The incidence of pericardial effusion and late cardiac tamponade after aortic and valvular surgery is higher than after other cardiac surgical procedures. The aim of this study is to evaluate the clinical safety and efficacy of prolonged mediastinal drainage using small, soft silastic drains (Blake drain, Ethicon USA) versus conventional mediastinal drainage using large chest tubes. A prospective randomized trial.