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Sinusitis clinical trials

View clinical trials related to Sinusitis.

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NCT ID: NCT00266474 Completed - Cystic Fibrosis Clinical Trials

Prevalence of Chronic Rhinosinusitis in Cystic Fibrosis

Start date: December 2005
Phase: N/A
Study type: Observational

Aim of the study is to detect the prevalence of chronic rhinosinusitis and the colonisation with Pseudomonas aerug. in the upper airways in patients with cystic fibrosis.

NCT ID: NCT00265434 Completed - Cystic Fibrosis Clinical Trials

Nasal Inhalation of Dornase Alfa (Pulmozyme) in Patients With Cystic Fibrosis and Chronic Rhinosinusitis

Start date: December 2005
Phase: Phase 3
Study type: Interventional

Rhinosinusitis disorders are often associated with Cystic Fibrosis. They can restrict quality of life enormously and give cause to repeated ENT surgery. The basic defect in CF is a dysfunction of Chloride channels in exocrine glands, leading to retention of secretions and consecutive chronic inflammation with bacterial superinfections. The prospective placebo controlled cross-over study aims at the evaluation of the efficacy of a nasally inhalation of Pulmozyme with respect to mucus retention and resulting inflammation.

NCT ID: NCT00249210 Completed - Sinusitis Clinical Trials

A Study of the Safety and Effectiveness of Levofloxacin Compared With Amoxicillin/Clavulanate Potassium in the Treatment of Adults With Rapid Onset of Severe Inflammation/Infection of the Sinuses

Start date: August 1993
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of levofloxacin, an antibiotic, compared with amoxicillin/clavulanate potassium in the treatment of adults with rapid onset of severe inflammation/infection of the sinuses.

NCT ID: NCT00245427 Completed - Sinusitis Clinical Trials

Outcomes of Patients Not Responding to Antibiotics in the Community

Start date: December 2005
Phase: N/A
Study type: Interventional

A study to report the outcomes of patients who fail to respond to beta-lactam and macrolide antibiotics in the community

NCT ID: NCT00242437 Completed - Sinusitis Clinical Trials

Hemostatic Matrix in Endoscopic Sinus Surgery

Start date: October 2005
Phase: Phase 4
Study type: Interventional

Evaluating clinical performance of Hemostatic Matrix with bovine thrombin in achieving hemostasis in patients undergoing endoscopic sinus surgery.

NCT ID: NCT00236652 Completed - Maxillary Sinusitis Clinical Trials

A Study Evaluating the Safety and Efficacy of Treating Sinus Infection With Levofloxacin 750 mg for 5 Days.

Start date: November 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effectiveness and safety of a once-daily administration of 750 milligrams levofloxacin (an antibiotic) for five days, in treating bacterial sinus infections.

NCT ID: NCT00236522 Completed - Sinusitis Clinical Trials

A Comparison of the Safety and Efficacy of Two Different Regimens of Levofloxacin in the Treatment of Acute Bacterial Sinusitis(Sinus Infection) in Adults.

Start date: October 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effectiveness and safety of two antibiotic regimens in the treatment of acute bacterial sinusitis (sinus infection) in non-hospitalized adult patients. A 5-day course of 750 milligrams of levofloxacin given by mouth once daily will be compared to a 10-day course of 500 milligrams of levofloxacin given by mouth once daily.

NCT ID: NCT00232154 Completed - Sinusitis Clinical Trials

A Study To Measure The Level Of Drug In Nasal Tissue And Blood After Taking A Single 2g Dose Or 500mg Tablets For Up To

Start date: November 2005
Phase: Phase 2
Study type: Interventional

To measure the level of drug in nasal tissue and blood after taking a single 2g dose or 500mg tablets for up to 3 days.

NCT ID: NCT00231062 Completed - Chronic Sinusitis Clinical Trials

Clinical Evaluation to Confirm Safety and Efficacy of Sinuplasty in the Paranasal Sinuses (CLEAR)

Start date: April 2005
Phase: Phase 3
Study type: Interventional

A multi-center, non-randomized, prospective post-market evaluation of sinuplasty in paranasal sinuses.

NCT ID: NCT00208065 Completed - Migraine Clinical Trials

Evaluation of Histamine, CGRP and VIP as Markers for Activation of Trigeminal and Parasympathetic Nerve Fibers

Start date: May 2004
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to evaluate histamine, CGRP and VIP levels in saliva as biological markers for activation of trigeminal and parasympathetic nerve fibers in various clinical presentations of primary headaches compared to allergic rhinosinusitis and control populations.