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Sinusitis clinical trials

View clinical trials related to Sinusitis.

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NCT ID: NCT02110654 Completed - Asthma Clinical Trials

Comparison of Daily Mometasone Furoate Nasal Spray Alone Versus a Combination With Montelukast for Treatment of Chronic Rhinosinusitis With Asthma After Functional Endoscopic Sinus Surgery

Start date: June 2014
Phase: Phase 4
Study type: Interventional

1. objectives. To compare the efficacy and the safety of mometasone furoate nasal spray (MFNS; Nasonex 200μg, daily) alone versus a combination with montelukast (singulair 10mg, daily) in chronic rhinosinusitis (CRS) with asthma after functional endoscopic sinus surgery (FESS) for improvement the clinical control of CRS 2. the clinical hypotheses. The investigators hypothesize that postoperative combined montelukast and MFNS can better improve clinical control of CRS concomitant with asthma after FESS compared with MFNS alone. 3. study design This study is a 9-month randomized, open-label, controlled interventional study.

NCT ID: NCT02106793 Completed - Clinical trials for Chronic Rhinosinusitis

Mitomicin C for Prevention Postoperative Endoscopic Sinus Surgery Synechia and QOL in Chronic Rhinosinusitis

Start date: March 2015
Phase: Phase 3
Study type: Interventional

Primary objective - To compare the incidence of postoperative nasal synerchia between Mitomicin C and placebo in patients at 6 months after endoscopic sinus surgery - To validate the Thai version of disease-specific quality of life tool SNOT-22 Secondary objectives - To compare the clinical signs and symptoms of CRS in patients who receive Mitomicin C with those who receive placebo - To compare the disease-specific quality of life in patients who receive Mitomicin C with those who receive placebo - To compare the side effects of Mitomicin C versus placebo

NCT ID: NCT02097576 Withdrawn - Rhinosinusitis Clinical Trials

Manuka Honey Nasal Rinse Study

Start date: May 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether high-volume nasal rinses with a manuka honey/saline mixture will improve symptom scores, nasal endoscopic findings and CT scan findings compared to nasal saline rinse without manuka honey in patients with chronic rhinosinusitis. Manuka honey is a honey made from bees that drink the nectar from tea (manuka) trees in New Zealand. It has been shown to have antibacterial activity against common bacteria that cause chronic sinusitis.

NCT ID: NCT02079792 Completed - Sinusitis Clinical Trials

The Optimal Head Position for Distributing Topical Nasal Medication Using the Mucosal Atomization Device

Head Position
Start date: June 2014
Phase: Phase 4
Study type: Interventional

Chronic Rhinosinusitis (CRS) is a common disorder of the nose characterized by stuffy nose, discoloured nasal discharge, sinus congestion or pressure and decreased sense of smell, present for over twelve weeks. Anti-inflammatory steroid medication is often used to treat sinus inflammation in CRS. These steroids are sometimes delivered using a spray device that creates a mist to deliver steroid medication deep into the nose. However, the distribution and efficacy of sprayed medication can be affected by the position of the patient's head. This study aims to determine which of two head positions is best for delivering steroid to the sinuses.

NCT ID: NCT02077322 Completed - Sinusitis Clinical Trials

Rates of Middle Meatal Synechia Formation Following Functional Endoscopic Sinus Surgery

SYNECHIAE
Start date: March 2014
Phase: N/A
Study type: Interventional

Functional endoscopic sinus surgery (FESS) is the best method of surgically treating patients who suffer from sinus disease. Synechiae formation in the nose is the most common complication after sinus surgery. Synechiae describes the adhesion of two opposing mucosal surfaces in the nasal cavity that can cause scarring and obstruction of the nasal passage. Spacers are often inserted during surgery between nasal mucosal surfaces to prevent synechiae. The aim of this study is to see if a silastic spacer is more effective at reducing the formation of synechiae after sinus surgery than a merocel spacer.

NCT ID: NCT02071667 Withdrawn - Sinusitis Clinical Trials

Association of Periostin Levels and Chronic Sinusitis

Start date: September 2014
Phase: N/A
Study type: Observational

The purpose of this study is to see if a protein in blood, called periostin, can determine if patients have chronic sinusitis. This protein is in everyone's body, but the level of the protein may indicate certain conditions such as chronic sinusitis. The investigators are interested in testing levels of periostin to see if they are higher or lower than patients without chronic sinusitis, just as periostin is higher in patients with asthma. All patients enrolled in this study will have chronic sinusitis without asthma.

NCT ID: NCT02038166 Recruiting - Rhinosinusitis Clinical Trials

Nasal Potential Difference (NPD) Protocol in Chronic Rhinosinusitis

Start date: January 2015
Phase:
Study type: Observational

The purpose of this study is to determine if acquired (partial) Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) deficiency contributes substantially to the pathogenic mechanisms underlying Chronic Rhinosinusitis (CRS), creating a localized environment that impairs mucociliary clearance (MCC).

NCT ID: NCT01990820 Completed - Clinical trials for Rhinitis + Sinusitis, Pediatric Chronic Rhinosinusitis

Study for the Management of Pediatric Chronic Rhinosinusitis With or Without Balloon Sinuplasty

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

Chronic rhinosinusitis, a common diagnosis in children, remains a poorly understood disease. Adenoidectomy (surgery to take out the adenoid pads- infection fighting glands in the back of the throat) is performed since the adenoid pad may trap germs that enter a child's body and can get so swollen with bacteria that they become infected themselves. Functional endoscopic sinus surgery (FESS) and adenoidectomy are currently the most common surgeries performed on children with this disease. Another treatment is adenoidectomy and irrigation of the maxillary sinus without FESS. New technology has emerged using a balloon catheter to dilate (open) the sinus passage in addition to the adenoidectomy and irrigation. This study seeks to answer if children with chronic rhinosinusitis who undergo adenoidectomy with balloon dilation of the maxillary sinus passage and irrigation experience improved quality of life outcomes compared to children with chronic rhinosinusitis who undergo an adenoidectomy with maxillary sinus irrigation without dilation of the sinus passage.

NCT ID: NCT01988779 Completed - Clinical trials for Chronic Rhinosinusitis

Oral Versus Topical Antibiotics for Chronic Rhinosinusitis Exacerbations

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

The purpose of this study is to treat patients with a diagnosis of chronic rhinosinusitis (CRS) and a history of bilateral endoscopic sinus surgery during times of worsening symptoms and signs of acute infection on nasal endoscopy with one of two treatments: (1) oral antibiotics and twice daily intranasal saline irrigations or (2) oral placebo and twice daily intranasal antibiotic irrigations. The two treatments will be compared to see if there is any difference in patient outcomes. This will help guide treatment strategies for patients with CRS in the future.

NCT ID: NCT01955980 Completed - Rhinosinusitis Clinical Trials

Buparid/PARI SINUS Versus Budes® Nasal Spray in the Therapy of Chronic Rhinosinusitis

Start date: October 27, 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The study should create data for the selection of a clinically relevant endpoint to assess the potential of Buparid/PARI SINUS to postpone sinus surgery in patients with chronic Rhinosinusitis.