Medical University Of Vienna
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Vienna, Austria
Rare diseases
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A plain-language summary of the goals, design and what participants do
This clinical trial is focused on studying two diseases: Chronic Obstructive Pulmonary Disease (COPD) and Cystic Fibrosis (CF). The study will explore the effects of two medications, Levofloxacin and Piperacillin/Tazobactam, which are both given as a solution for infusion, meaning they are administered directly into the bloodstream through a vein. The purpose of the study is to compare different methods of measuring how these antibiotics behave in the lungs of patients with COPD or CF.
Participants in the study will receive either Levofloxacin or Piperacillin/Tazobactam as part of their treatment. The study will involve taking samples from the lungs to measure the concentration of the antibiotics. This will be done using three methods: collecting fluid from the lining of the lungs, taking a small tissue sample, and using a technique called in-vivo microdialysis, which involves measuring the drug concentration in the body over a period of time. These methods will help researchers understand how the drugs are distributed in the lungs.
The study will be conducted over a short period, with the main focus on comparing the three methods of measurement. The results will provide valuable information on how these antibiotics work in the lungs of patients with Chronic Obstructive Pulmonary Disease and Cystic Fibrosis, potentially leading to better treatment strategies in the future.
The trial runs in 4 steps – from screening to follow-up. Each step says what happens and what the team monitors.
4 criteria
2 criteria
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Vienna, Austria
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is a combination of two medications used to treat bacterial infections. Piperacillin is an antibiotic that helps kill bacteria, while Tazobactam is a substance that prevents bacteria from breaking down the antibiotic, making it more effective. In this trial, the medication is being studied to understand how it moves and is absorbed in the lungs of patients with chronic obstructive pulmonary disease (COPD) or cystic fibrosis.
is an antibiotic used to treat a variety of bacterial infections. It works by stopping the growth of bacteria. In this clinical trial, researchers are examining how Levofloxacin is distributed and absorbed in the lungs of patients with COPD or cystic fibrosis. This study aims to compare different methods of measuring how the drug behaves in the body.
This medication is administered intravenously, meaning it is given directly into a vein through an injection or infusion. It is currently used in medicine to treat infections, and its effectiveness is being studied in patients with chronic obstructive pulmonary disease (COPD) and cystic fibrosis. The main therapeutic use of piperacillin/tazobactam is to fight bacterial infections by stopping the growth of bacteria. At the molecular level, it works by inhibiting the formation of bacterial cell walls, which are essential for their survival. It belongs to the pharmacological class of antibiotics known as beta-lactam antibiotics.
This medication is taken orally in the form of tablets or administered intravenously, depending on the patient's needs. It is widely used in medicine to treat a variety of bacterial infections, and its use is being explored in patients with chronic obstructive pulmonary disease (COPD) and cystic fibrosis. Levofloxacin's main therapeutic role is to eliminate bacteria by interfering with their DNA replication process, which is crucial for their growth and multiplication. It is classified as a fluoroquinolone antibiotic, a group of drugs known for their broad-spectrum antibacterial activity.
Chronic Obstructive Pulmonary Disease (COPD) is a long-term lung condition that obstructs airflow from the lungs. It is characterized by breathing difficulties, cough, mucus production, and wheezing. The disease progresses slowly, with symptoms worsening over time. In COPD, the airways and air sacs lose their elastic quality, and the walls between many of the air sacs are destroyed. The walls of the airways become thick and inflamed, and the airways produce more mucus than usual, which can clog them. This leads to reduced airflow and difficulty in breathing.
Cystic Fibrosis is a genetic disorder that affects the respiratory and digestive systems. It is characterized by the production of thick, sticky mucus that can clog the airways and lead to severe respiratory and digestive problems. The disease progresses as the thick mucus builds up, causing blockages and infections in the lungs and other organs. Over time, this can lead to lung damage and respiratory failure. In the digestive system, the mucus can block the ducts of the pancreas, preventing digestive enzymes from reaching the intestines. This results in difficulty absorbing nutrients and poor growth.
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