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Pleural Effusion, Malignant clinical trials

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NCT ID: NCT03272997 Completed - Clinical trials for Pleural Effusion, Malignant

The Value of PET-CT in Pleural Effusions

Start date: October 1, 2017
Phase:
Study type: Observational

The investigators aim is to asses the diagnostic power of 18F-FDG PET-CT in discriminating malignant from nonmalignant causes in patients with a recurrent unilateral pleural effusion of unknown origin.

NCT ID: NCT03270215 Completed - Clinical trials for Pleural Effusion, Malignant

The Added Value of CT Scanning in Patients With an Unilateral Pleural Effusion

Start date: October 1, 2017
Phase:
Study type: Observational

To investigate the diagnostic power of computed tomography for discriminating malignant from nonmalignant causes to pleural effusions in consecutive patients with no malignant cells found at a cytological examination and a chest x-ray not suspicious of malignancy. The investigators hypothesised that the combination improves the chance of detecting the cause of the pleural effusion.

NCT ID: NCT02674243 Completed - Clinical trials for Malignant Pleural Effusion

Efficacy of Iodopovidone Versus Talc in Palliative Malignant Pleural Effusion

Start date: November 2015
Phase: Phase 3
Study type: Interventional

This is prospective randomized control trial study. The aim of this study is to evaluate the efficacy of Iodopovidone solution for pleurodesis in palliative malignant pleural effusion (MPE) patients comparing to Talc. All adult patients who diagnosed MPE by cytology regardless primary tumor between December 1, 2015 and November 29, 2016 at Maharaj Nakorn Chiang Mai Hospital, Chiang Mai University, Chiang Mai, Thailand will be enrolled in this study. The inform and consent will be applied in all patients before treatment. Patients will be randomized to two groups; Iodopovidone group (intervention group) and Talc group (control group)

NCT ID: NCT02649894 Completed - Clinical trials for Malignant Pleural Effusion

Safety and Effectiveness of a New Pleural Catheter for Symptomatic, Recurrent, MPEs Versus Approved Pleural Catheter

SWIFT
Start date: May 2016
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 compared to approve catheter.

NCT ID: NCT02625675 Completed - Clinical trials for Malignant Pleural Effusion

Using Thoracic Ultrasound to Predict Pleurodesis Success in Malignant Pleural Effusions: a Pilot Study

Start date: March 19, 2015
Phase: N/A
Study type: Observational

The observational pilot study at the Churchill Hospital, funded by Oxford Respiratory Trials Unit, will assess the feasibility and efficacy of thoracic ultrasound (TUS) assessment in patients undergoing talc pleurodesis via intercostal chest drain (ICD) for recurrent symptomatic malignant pleural effusions (MPE). Participants will undergo TUS pre and post pleurodesis on up to four occasions. We hypothesise that a TUS scoring system will be able to predict short and long-term pleurodesis success earlier than current conventional medical practice allows. This study may ultimately allow the proposal of a treatment algorithm to manage patients with MPE in a more efficient manner.

NCT ID: NCT02583282 Completed - Clinical trials for Malignant Pleural Effusion

A Study to Compare the Efficacy and Safety of Intrapleural Doxycycline Versus Iodopovidone for Performing Pleurodesis in Malignant Pleural Effusion

Start date: August 1, 2015
Phase: N/A
Study type: Interventional

Malignant pleural effusion (MPE) arises in advanced-stages of malignancies and frequently heralds a poor prognosis.If the underlying malignancy is chemo sensitive (e.g., small-cell carcinoma of lung & lymphoma), systemic chemotherapy may control the pleural effusion. Instilling of sclerosing agents into the pleural cavity (pleurodesis) is a common method for the management of MPE. According to a recent survey, tetracycline or its derivative (doxycycline) is the preferred agent for performing pleurodesis at many centers. In a previous study from the investigators' center, the investigators have demonstrated equal efficacy of iodopovidone in comparison to talc in inducing pleural symphysis. Also, iodopovidone has been postulated to have anti-neoplastic effects and hence may help in reducing the drain output. Apart from these benefits iodopovidone is easily available and is cost effective. The investigators believe that iodopovidone will have better efficacy than doxycycline in inducing pleurodesis in malignant pleural effusion.

NCT ID: NCT02517749 Completed - Clinical trials for Pleural Effusion, Malignant

Out Patient Talc Slurry Via Indwelling Pleural Catheter for Malignant Pleural Effusion Vs Usual Inpatient Management

OPTIMUM
Start date: August 2015
Phase: N/A
Study type: Interventional

This is a multicentre randomised controlled trial evaluating global health related quality of life outcomes in patients with malignant pleural effusions. Patients will be randomised to receive either chest drain and talc pleurodesis or indwelling pleural catheter and talc pleurodesis. Patients will be followed up for 3 months post intervention

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: 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: 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.