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Hemoptysis clinical trials

View clinical trials related to Hemoptysis.

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NCT ID: NCT04771923 Completed - Bleeding Clinical Trials

Tranexamic Acid Versus Adrenaline for Controlling Iatrogenic Endobronchial Bleeding

TAVA
Start date: February 22, 2021
Phase: N/A
Study type: Interventional

Endobronchial bleeding is a relatively common complication of diagnostic bronchoscopy. Both tranexamic acid and adrenaline are used topically for the control of endobronchial bleeding. The aim of this study is to compare the efficacy of tranexamic acid with adrenaline in controlling iatrogenic endobronchial bleeding after diagnostic bronchoscopy.

NCT ID: NCT04770675 Completed - Pulmonary Disease Clinical Trials

Post Market Study to Collect Data for Software Recognizing the Anatomical Structures During Bronchoscopy.

Start date: December 1, 2020
Phase:
Study type: Observational

The primary aim is to develop a software algorithm that has the capacity to detect the normal 18 anatomical structures of the lung by using the position of the scope during the bronchoscopy procedure and using existing bronchoscopy technology.

NCT ID: NCT04555564 Withdrawn - Lung Cancer Clinical Trials

Tc99m Macroaggregated Albumin Bronchial Artery Study

Start date: August 1, 2022
Phase: N/A
Study type: Interventional

This is a single-arm, single-center, prospective pilot study to perform bronchial artery Tc-99m-MAA infusion to determine the predicted whole lung versus lung tumor dosimetry of a possible intra-arterial radioembolization.

NCT ID: NCT04105283 Recruiting - Lung Cancer Clinical Trials

Tc99m-MAA Bronchial Artery Injection During Bronchial Embolization for Pulmonary Mass Induced Hemoptysis for Dosimetry Planning

Start date: August 1, 2020
Phase: Phase 1
Study type: Interventional

This research study will evaluate the administration of a particle called macro-aggregated albumin (MAA) labelled with the radiotracer technetium 99m (Tc99m) as a proxy to estimate the anticipated dose of radiation to tumor and adjacent structures. Administration of this labeled MAA will not have a therapeutic benefit on the participant's cancer. Administration will help researchers determine if arterial administration of radiation may be feasible for lung cancer in the future.

NCT ID: NCT04087135 Completed - Clinical trials for Intubation; Difficult or Failed

Comparison of Intubation With Direct Laryngoscopy or Videolaryngoscopy in an Hemoptysis Simulated Situation on Human Cadaver Embalmed With Thiel's Method

Start date: March 11, 2019
Phase: N/A
Study type: Interventional

Our study first aims to develope a realistic cadaver model of hemoptysis based on Thiel's embalmed cadavers. Secondly, participants will intubate the hemoptysis cadaver model with (a) the direct laryngoscopy with MacIntosh blade, (b) the videolaryngoscopy with McGrath XBlade and (c) the videolaryngoscopy with McGrath XBlade and a suction advance before the optic of the camera. We hypothesis that, in simulated hemoptysis on the Thiel's embalmed cadaver, the rate of failed intubation at first try will be different depending on the laryngoscope used.

NCT ID: NCT04079400 Completed - Lung Cancer Clinical Trials

Microbiome in Pulmonary Tuberculosis, Non-tuberculous Mycobacterial Pulmonary Diseases, Lung Cancer and Hemoptysis

Start date: December 1, 2016
Phase:
Study type: Observational [Patient Registry]

Microbiome in lower respiratory diseases is not sufficiently known yet. The objective of this study is to investigate microbiome in patients who present with hemoptysis, and those with pulmonary tuberculosis, non-tuberculous mycobacterial pulmonary disease (NTM-PD), and lung cancer, analyzing respiratory specimen acquired by bronchoscopic approach.

NCT ID: NCT03824366 Completed - Metastasis Clinical Trials

Same-session MR-only Simulation and Treatment With MRI-guided Adaptive Palliative RadioTherapy

MAP-RT
Start date: April 23, 2019
Phase: N/A
Study type: Interventional

This proposed study is unique in that patients will not undergo computed tomography (CT) simulation at any point during their treatment course and will instead have same-session magnetic resonance (MR)-only simulation and treatment planning, on-table, using the adaptive radiotherapy (ART) workflow. In this manner, patients requiring urgent treatment could initiate treatment as early as the day of initial radiation oncology consultation.

NCT ID: NCT03625947 Terminated - Cancer Clinical Trials

Efficacy and Safety of Argon Plasma Coagulation in the Treatment of Patients With Hemoptysis Caused by Endobronchial Malignancies

Start date: August 8, 2018
Phase:
Study type: Observational

The aim of this study is to evaluate the efficacy, the safety and the main predictors of success of bronchoscopic Argon Plasma Coagulation in patients with hemoptysis caused by endobronchial malignancies.

NCT ID: NCT03270735 Recruiting - Hemoptysis Clinical Trials

A Clinical Study to Evaluate the Efficacy and Safety of Hemocoagulase Injection

Start date: June 6, 2017
Phase: Phase 4
Study type: Interventional

This is a multi-centre, randomised, double blind, placebo controlled clinical study which is designed to evaluate the efficacy and safety of hemocoagulase in the treatment of moderate to severe hemoptysis.

NCT ID: NCT03126968 Completed - Bleeding Clinical Trials

Prophylactic Topical Epinephrine to Reduce Bleeding in Transbronchial Lung Biopsies

PROPHET
Start date: July 1, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

Bleeding poses potential for significant complication after transbronchial lung biopsies. The investigators hypothesize that prophylactic intrabronchial instillation of topical epinephrine will reduce the likelihood of bleeding. The investigators plan a double-blind, placebo controlled trial to evaluate this hypothesis.