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Sinusitis clinical trials

View clinical trials related to Sinusitis.

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NCT ID: NCT01155752 Withdrawn - Cystic Fibrosis Clinical Trials

Pulmozyme in Cystic Fibrosis With Sinusitis

Start date: July 2013
Phase: Phase 3
Study type: Interventional

The hypothesis is that the intranasal use of Pulmozyme will decrease the severity of sinusitis in Cystic Fibrosis and lead to an improved quality of life.

NCT ID: NCT01146860 Completed - Clinical trials for Acute Rhinosinusitis

Efficacy and Safety of a Herbal Medicinal Product (Dry Extract BNO 1016) in Patients With Acute Rhinosinusitis

Start date: January 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the dry extract BNO 1016 is effective and safe in the treatment of acute rhinosinusitis in adults.

NCT ID: NCT01129765 Completed - Allergic Rhinitis Clinical Trials

Home Usability of a Nasal Lavage System in Children

Start date: July 2009
Phase: N/A
Study type: Observational

This study evaluates labeling comprehension, ease of use and effectiveness of a new device for nasal and sinus irrigation and/or aspiration. The device is currently cleared for professional use and home use with a prescription. This is a usability study to demonstrate that this device is appropriate for home use.

NCT ID: NCT01118312 Completed - Asthma Clinical Trials

Study of Asthma and Nasal Steroids

STAN
Start date: September 2010
Phase: Phase 4
Study type: Interventional

The trial will study the effectiveness of nasal steroids for the treatment of chronic rhinitis and/or sinusitis on asthma control.

NCT ID: NCT01115309 Completed - Sinusitis Clinical Trials

XprESS Registry Study

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

This is a prospective, non-randomized, multi-center study to assess safety and long-term patency of the ostia treated with the XprESS device per the device indication for use (IFU).

NCT ID: NCT01107379 Completed - Sinusitis Clinical Trials

Optimization and Refinement of Technique in In-Office Sinus Dilation 2

ORIOS 2
Start date: April 2010
Phase: N/A
Study type: Observational

A prospective, multi-arm, multi-center, observational post-market study of balloon sinus dilatation in the physician office setting under local anesthesia to treat patients with chronic rhinosinusitis (CRS). All products intended for use in this study have been FDA cleared for sale in the U.S.A.

NCT ID: NCT01086839 Completed - Cystic Fibrosis Clinical Trials

Sino-nasal Inhalation of Sodium Chloride 6,0% in Patients With Cystic Fibrosis and Chronic Rhinosinusitis

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

Rhinosinusitis disorders are almost regularly associated to Cystic Fibrosis (CF). The basic defect in CF is a dysfunction of chloride channels in exocrine glands which equally concerns upper airway mucosa. It leads to retention of secretions and consecutive chronic inflammation with bacterial superinfection. In CF rhinosinusitis can restrict quality of life, give cause to repeated ear, nose, and throat (ENT) surgery and accelerate disease progression by bacterial acquisition into the airways. The multicenter, randomized, double-blind, placebo-controlled, prospective clinical trial aims at the evaluation of a sino-nasal inhalation of sodium chloride 6% compared to isotonic saline with respect to ENT-related quality of life which is influenced by mucus retention and the resulting inflammation.

NCT ID: NCT01084811 Recruiting - Clinical trials for Chronic Rhinosinusitis

Chronic Rhinosinusitis: Biochemical Markers and Biofilm

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

The investigators will conduct a descriptive, prospective, three-armed study concerning the pathophysiology of chronic rhinosinusitis. In one part of the study the investigators want to investigate the presence of biofilm in patients with chronic rhinosinusitis both with and without nasal polyps compared with a control group of subjects without chronic rhinosinusitis. The investigators will also compare quality of life in the three groups and correlate disease severity in biofilm patients versus patients where biofilm was not present. The hypothesis here is that biofilm patients suffers a more severe disease. In the other arm of the study the investigators will compare the presence of different biochemical compounds in the three study groups. The investigators specifically want to investigate matrix metalloproteases and apoptosis-inhibitors with immunohistochemistry. The investigators may also add other compounds to our test-battery if interesting candidates surface in the literature during the inclusion period. The purpose of this part of the study is to investigate candidates for the development of nasal polyposis. The investigators plan to include 100 patients suffering from chronic rhinosinusitis with nasal polyps, and 100 patients with chronic rhinosinusitis without nasal polyps and 30 control subjects.

NCT ID: NCT01066416 Terminated - Asthma Clinical Trials

Effects of Endoscopic Sinus Surgery for Chronic Sinusitis on Asthma Control

Start date: July 2009
Phase: N/A
Study type: Interventional

It is unknown whether surgical treatment of chronic sinusitis improves asthma control in patients with poorly controlled asthma. This is a randomized trial of surgical plus medical sinus therapy versus medical therapy alone.

NCT ID: NCT01066104 Completed - Clinical trials for Chronic Rhinosinusitis

Subcutaneous Omalizumab for Treatment of Chronic Rhinosinusitis With Nasal Polyposis

Xolair CRS
Start date: December 2009
Phase: Phase 2
Study type: Interventional

The investigators are doing this research study to learn more about a drug called Xolair (omalizumab). The investigators want to see if it is an effective treatment for chronic rhinosinusitis (CRS). Specifically, the investigators want to see whether Xolair will make nasal polyps smaller and less thick, and relieve symptoms in people with CRS. Polyps are abnormal growths of tissue that can grow in the lining of your sinuses (the inside of your nose). The investigators also want to find out if it is safe to use (whether it causes side effects).