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Pulmonary Aspergillosis clinical trials

View clinical trials related to Pulmonary Aspergillosis.

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NCT ID: NCT01710930 Completed - Clinical trials for Allergic Broncho-Pulmonary Aspergillosis

Protocol TARC-ABPA

Start date: July 2012
Phase: N/A
Study type: Interventional

The main objective of this study is to determine if a doubling of serum TARC (compared to baseline) is associated with the occurrence of exacerbations of ABPA. The secondary objectives of the study are : 1. To investigate if induced sputum eosinophils count (compared to baseline) is associated with the occurrence of exacerbations. 2. To examine if the exhaled NO (compared to a baseline) is associated with the occurrence of exacerbations. 3. To investigate if activation of circulating T cells (compared to a baseline) is associated with the occurrence of exacerbations. 4. To examine if the rate of specific Asp f IgG measured by ELISA (compared to a baseline) is associated with the occurrence of exacerbations. 5. To determine if the variation of one of the markers above, TARC or Asp f specific IgE measured at baseline, may be associated with the radiological stage of the disease (ABPA-S, ABPA-CB, ABPA-ORF). 6. To investigate if there is a link between fungal exposure at home (visually assessed by the contamination level and the proportion of positive samples for Asp. f) and the frequency of exacerbations. 7. To establish if some of the clinical, functional or biological data studied are associated with the frequency of exacerbations.

NCT ID: NCT01621321 Completed - Clinical trials for Allergic Bronchopulmonary Aspergillosis

Voriconazole Versus Oral Steroids in Allergic Bronchopulmonary Aspergillosis

Start date: June 2013
Phase: Phase 2/Phase 3
Study type: Interventional

This is a research project to evaluate the efficacy and safety of two different treatment protocols in Allergic bronchopulmonary Aspergillosis.

NCT ID: NCT01615809 Completed - Clinical trials for Invasive Pulmonary Aspergillosis

Nebulized Amphotericin B Lipid Complex in Invasive Pulmonary Aspergillosis in Paediatric Patients With Acute Leukaemia

Start date: October 2011
Phase: Phase 2
Study type: Interventional

The trial evaluates the overall tolerability of the drug and the efficacy of aerosolised amphotericin B as a lipid complex (ABLC) for primary prophylaxis of invasive pulmonary aspergillosis (IPA) in pediatric patients with acute leukemia undergoing intensive chemotherapy.

NCT ID: NCT01499433 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Efficacy and Safety of Caspofungin for Invasive Pulmonary Aspergillosis Underlying Chronic Obstructive Pulmonary Disease

Start date: January 2012
Phase: Phase 4
Study type: Interventional

The investigators propose to study the efficacy and safety of three-week antifungal therapy with caspofungin in hospitalized patients with proven or probable IPA underlying chronic obstructive pulmonary disease.

NCT ID: NCT01430663 Completed - Clinical trials for Invasive Aspergillosis

Diagnosing Pulmonary Aspergillosis in Patients With Hematological Malignancies: A Multicentre Prospective Evaluation of an Aspergillus PCR Assay and a Galactomannan ELISA in Bronchoalveolar Lavage Samples

Start date: April 2007
Phase:
Study type: Observational

Diagnosing invasive pulmonary aspergillosis (IPA) remains a challenge in patients (pts) with hematological malignancies. The clinical significance of testing bronchoalveolar lavage (BAL) samples both with polymerase chain reaction (PCR) and Aspergillus galactomannan (GM) ELISA is unclear, and the BAL cutoff for GM has not been clearly defined yet. Using a validated nested PCR assay and a GM ELISA, we prospectively examine BAL samples from hematological patients at high risk of PA.

NCT ID: NCT01321827 Completed - Clinical trials for Allergic Bronchopulmonary Aspergillosis

Monotherapy of Itraconazole Versus Prednisolone in Allergic Bronchopulmonary Aspergillosis

MIPA
Start date: April 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of itraconazole monotherapy in patients with ABPA.

NCT ID: NCT01301755 Recruiting - Immunocompromised Clinical Trials

Diagnosis of Invasive Pulmonary Aspergillosis by Direct Lung Tissue Aspergillus Galactomannan Antigen Detection From Aspirate by Ultrasound-guided Fine Needle Aspiration

Start date: March 2010
Phase: N/A
Study type: Observational

Invasive aspergillosis is a serious and often fatal infection in patients who are neutropenic or have undergone solid organ or stem cell transplantation. However, early diagnosis of invasive aspergillosis is a challenge. Reiss and Lehmann first described the value of serum Galactomanna (GM) for diagnosis of invasive pulmonary aspergillosis in 1979. The availability of the Platelia Aspergillus, a sandwich ELISA that has been approved by FDA in 2003 for managing patients at risk of invasive aspergillosis because of the early detection of the GM antigen. In several studies so far the specificity of the serum galactomannan assay was greater than 85%; however, variable sensitivity from 29~100% was noted over years. In addition, low values and false-negative results are seen more often in nonneutropenic and solid organ transplantation patients as opposed to severely granulocytopenic patients .There are several factors that might explain the reported difference in the performance of antigen detection, including the biological factors and epidemiological factors. In recent years, specimens of other body fluids are increasingly used for detection of Aspergillus galactomannan antigen, including urine, bronchoalveolar lavage(BAL) fluid, cerebrospinal fluid and even the tissue specimen. However, the sensitivity and specificity of the GM detection in various specimens still have considerably variation. Ultrasound-guided transthoracic aspirate is a safe and useful method for collecting specimens for accurate bacteriologic diagnosis of lung abscess and obstructive pneumonitis10. We also reported a study of diagnosis of pulmonary Cryptococosis by ultrasound guided percutaneous aspiration. We plan to perform a prospective single-center study to investigate the role of GM in the target organ (lung tissue/fluid) by using ultrasound-guided fine needle aspirate for early diagnosis invasive aspergillosis compared with the serum galactomannan.

NCT ID: NCT01259336 Completed - Clinical trials for Chronic Cavitary Pulmonary Aspergillosis

Efficacy Of Itraconazole In Chronic Cavitary Pulmonary Aspergillosis

ITRACONASP
Start date: July 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether there itraconazole is effective in the treatment of chronic cavitary pulmonary aspergillosis

NCT ID: NCT01247142 Completed - Clinical trials for Invasive Pulmonary Aspergillosis

Evaluation of Exhaled Breath Condensate in the Diagnosis of Invasive Pulmonary Aspergillosis

Start date: January 2011
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the diagnostic potential of biomarkers for invasive pulmonary aspergillosis in exhaled breath condensate.

NCT ID: NCT01222273 Completed - Cystic Fibrosis Clinical Trials

Open-label Vitamin D Trial for Patients With Cystic Fibrosis and Allergic Bronchopulmonary Aspergillosis

Start date: September 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to see if giving people with CF and ABPA enough vitamin D to make their blood levels of the vitamin higher, will reduce the allergic response in their body and make the symptoms caused by ABPA better.