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Chronic Sinusitis clinical trials

View clinical trials related to Chronic Sinusitis.

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NCT ID: NCT01608308 Completed - Chronic Sinusitis Clinical Trials

Intraoperative and Post-operative Analgesic Effect of IV Acetaminophen for Sinus Surgery

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

The purpose of this study is to assess the use of IV acetaminophen (Ofirmev) as a and safe and efficacious agent in reducing post-operative pain; we hypothesize that its use will reduce post-operative pain when compared to a control group using the visual analogue score (VAS) analog pain scoring system.

NCT ID: NCT01569048 Completed - Chronic Sinusitis Clinical Trials

Randomized Controlled Trial to Evaluate of Dexmedetomidine for the Effect on Operative Visibility in Patients Undergoing Endoscopic Sinus Surgery

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

Various maneuvers are commonly used to achieve the ideal operative field necessary for successful endoscopic sinus surgery (ESS). Dexmedetomidine, a potent alpha2 adrenoceptor agonist which dose-dependently reduces arterial blood pressure and heart rate, decreases the hemodynamic and catecholamine response. And dexmedetomidine has an effect of peripheral vasoconstriction thus it is thus theologically appropriate for reducing bleeding during intranasal operation. The aim of this study is to compare the effect of dexmedetomidine, an alpha2-adrenoreceptor agonist, on intraoperative bleeding, propofol requirement and postoperative profiles to remifentanil , an ultrashort-acting opioid.

NCT ID: NCT01564355 Completed - Chronic Sinusitis Clinical Trials

Postoperative Systemic Corticosteroids When Utilizing a Steroid-Eluting Spacer Following Endoscopic Sinus Surgery

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

Chronic rhinosinusitis (CRS) is an inflammatory condition of the nose and sinuses. It affects about 5 to 10% of Canadians. Patients suffer from congestion in the nose and sinuses, nasal discharge, pressure in the face, and a reduced sense of smell. This affects people's enjoyment of life. Medical management uses sprays or pills to treat these symptoms but for some patients sinus surgery is needed. This type of surgery is called endoscopic sinus surgery (ESS). There is no single correct approach to take care of patients after sinus surgery. Most experts would use a nasal spray and a short-course of oral steroid pills to reduce sinus swelling and minimize complications related to scarring. "Steroid-eluting nasal spacers" are devices placed inside the sinus during surgery and slowly release topical steroids into the sinuses better than steroid sprays. These "spacers" have been shown to improve results following sinus surgery. When using these special "spacers", there may no longer be a need for oral steroid pills following surgery. This would help to avoid potential side effects associated with these medications. The purpose of this study is to find out whether taking oral (systemic) steroid pills following sinus surgery is necessary to improve surgical results, now that steroid-eluting nasal spacers are commonly used during surgery.

NCT ID: NCT01525862 Completed - Chronic Sinusitis Clinical Trials

XprESS Maxillary Balloon Dilation Study

Start date: December 2011
Phase: N/A
Study type: Interventional

A prospective, single-arm, post approval pilot study.

NCT ID: NCT01525849 Completed - Chronic Sinusitis Clinical Trials

Randomized Evaluation of Maxillary Antrostomy Versus Ostial Dilation Efficacy Through Long-Term Follow-Up

REMODEL
Start date: December 2011
Phase: N/A
Study type: Interventional

The objective of this study is to show that long-term symptom improvement following sinus balloon dilation is not worse than symptom improvement following functional endoscopic sinus surgery.

NCT ID: NCT01430026 Completed - Chronic Sinusitis Clinical Trials

Efficacy and Complication of Gentamicin Nasal Irrigation in Chronic Rhinosinusitis

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

The propose of this study to determine efficacy and complication of gentamicin nasal irrigation in chronic rhinosinusitis

NCT ID: NCT01253577 Completed - Chronic Sinusitis Clinical Trials

A Clinical Evaluation of a Steroid-Coated Sinus Stent When Used Following Functional Endoscopic Sinus Surgery in Patients With Chronic Sinusitis

ADVANCE II
Start date: December 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of the Propel mometasone furoate implant when used following Functional Endoscopic Sinus Surgery (FESS) in patients with Chronic Sinusitis (CS).

NCT ID: NCT01197612 Completed - Chronic Sinusitis Clinical Trials

Nasal Packing as a Drug Delivery System Postoperatively in Chronic Sinusitis With Polyposis

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

That high-dose steroid applied to the nasal cavity immediately post-operatively will improve olfaction and healing following endoscopic sinus surgery.

NCT ID: NCT01007799 Completed - Chronic Sinusitis Clinical Trials

Vitamin D for Chronic Sinusitis

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

The purpose of this study is to examine if vitamin D improves the symptoms of chronic sinusitis.

NCT ID: NCT00962689 Completed - Chronic Sinusitis Clinical Trials

Clinical Study to Improve Diagnosis and Treatment of Sinusitis

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

Chronic rhinosinusitis (CRS) is the most common chronic medical condition that affects Americans between 18-44 years of age. While significant advances have been made in the understanding of the molecular pathogenesis underlying many subtypes of CRS, this has not translated into widespread changes in how physicians manage adult or pediatric CRS. The focus of this study is intended to develop testing methods to improve the objectivity and specificity of diagnosis and allow for individualized therapy with less invasive, customized treatments instead of the traditional, empiric based, and radically exenterative therapies commonly employed in clinical practice. Specifically, it is now known that many patients with CRS have a greater concentration of non-typeable Haemophilus influenzae (NTHI) in the bacterial biofilms located within their sinus cavities compared to healthy patients. The specific hypothesis behind the proposed research is that the presence of NTHI biofilms, which are known to be highly recalcitrant, are positively correlated with the development of CRS and that unique lipooligosaccharides and inflammatory byproducts obtained from nasopharyngeal lavage fluids and/or swabs of sinus secretions may be used as a non-invasive biomarker for CRS. As a result, patients with symptoms of CRS specifically associated with NTHI biofilms could possibly obtain a non-invasive test in the physician's office that would allow the clinician to make a more accurate diagnosis and objectively follow each patient's responsiveness to customized therapy.