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Chronic Sinusitis clinical trials

View clinical trials related to Chronic Sinusitis.

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NCT ID: NCT03729310 Withdrawn - Chronic Sinusitis Clinical Trials

Comparison of Two Steroid Nasal Implants Following Endoscopic Sinus Surgery for Chronic Rhinosinusitis

Start date: March 2020
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to learn whether there is a difference in postoperative (after surgery) endoscopic appearance of the sinus cavities (the way that the sinuses look through a camera) between sinuses that receive one of two types of resorbable steroid eluting sinus packing (a sponge-like material which dissolves within several days while releasing a steroid): 1) Propel Implant or 2) Nasopore soaked with triamcinolone at the time of endoscopic sinus surgery (ESS) for chronic rhinosinusitis.

NCT ID: NCT03519061 Withdrawn - Chronic Sinusitis Clinical Trials

Impact of Budesonide Irrigations on Patients With Chronic Rhinosinusitis and Impact on Sinus Surgery Rates

Start date: August 13, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

This study is intended to assess the impact of a 90 day course of high volume budesonide irrigations for patients who have failed other medical therapy and assessing the impact of the budesonide irrigations on the need for sinus surgery.

NCT ID: NCT02981017 Withdrawn - Chronic Sinusitis Clinical Trials

Improvement of Outcomes in Draf III/Endoscopic Modified Lothrop Procedure

Start date: November 1, 2016
Phase: N/A
Study type: Interventional

We propose a randomized, single-blinded, prospective trial in order to evaluate the efficacy of the Cook Biodesign ENT Repair graft in improving outcomes after the Draf III or Endoscopic Modified Lothrop procedure. The Cook Biodesign ENT Repair graft is a porcine intestinal submucosal xenograft which has been FDA approved for use as an adjunct to natural healing process in the sinonasal cavity. The Draf III or Endoscopic Modified Lothrop involved creating a large unified drainage pathway for refractory frontal sinusitis. After the procedure is completed, there is exposed bone along the frontal beak region which can become a nidus for inflammation, crusting and eventual scarring, leading to stenosis or even complete blockage of the frontal sinuses. The Cook Biodesign will be used to cover this exposed bone in order to potentially reduce the inflammation, crusting and scarring and possibly improve outcomes.

NCT ID: NCT01185808 Withdrawn - Chronic Sinusitis Clinical Trials

Vitamin D Supplementation in Chronic Rhinosinusitis With Nasal Polyps

VDinCRS
Start date: October 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if Vitamin D supplementation improves clinical and immunologic parameters in chronic rhinosinusitis with nasal polyps.

NCT ID: NCT00841802 Withdrawn - Nasal Polyps Clinical Trials

Chronic Rhinosinusitis With or Without Nasal Polyps Steroid Study

Start date: July 2008
Phase: Phase 4
Study type: Interventional

This is a study to evaluate the cause of chronic sinus disease. Oral steroids have long been used in the treatment of inflammatory conditions including chronic sinusitis, asthma, and arthritis. However, it is not well known exactly which patients will benefit from steroids when used in the treatment of chronic sinusitis. For some doctors, it is common practice to use these medications prior to planned sinus surgery, to lessen the inflammation and possibly help the healing process. Other doctors feel oral steroids may not be helpful in this way, and there is no conclusive data as to whether this practice has a long term benefit.

NCT ID: NCT00705354 Withdrawn - Sinusitis Clinical Trials

Pilot Study To Evaluate A Pharmacologically Active Nasal Sponge Following Endoscopic Sinus Surgery

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

This study will compare the incidence of post-op infection after sinus surgery using conventional post-op oral antibiotics to the incidence of infection after sinus surgery when a bio-resorbable antibiotic soaked nasal sponge is used in the nasal cavity in lieu of post-op oral antibiotics. The nasal sponge is a routine nasal dressing used after sinus surgery and will therefore be placed in all patients.

NCT ID: NCT00671541 Withdrawn - Chronic Sinusitis Clinical Trials

Nasospore Stent For Use in Enodscopic Sinus Surgery

Start date: March 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate a stenting material called Nasopore. This is a synthetic material approved by FDA for use as a stent in postoperative sinus surgery patients. This study will compare the Nasopore stent to other approved stenting materials.

NCT ID: NCT00671281 Withdrawn - Chronic Sinusitis Clinical Trials

The Effect of Tranexamic Acid on Intraoperative and Post-Operative Bleeding in Functional Endoscopic Sinus Surgery

Start date: October 2008
Phase: N/A
Study type: Interventional

Sinus surgery is a common, day surgery procedure performed by general and subspecialty trained otolaryngologists. In most cases, this is a safe surgery with a low incidence of complications. When there is significant bleeding or enough bleeding to obscure important anatomical landmarks, there is a higher chance of complications. These complications can include blindness, meningitis or cerebrospinal fluid leak. Our hypothesis is that in patients taking oral tranexamic acid three days before surgery and six days after, there will be less intraoperative bleeding, better surgical visualization and less postoperative bleeding events.

NCT ID: NCT00603785 Withdrawn - Chronic Sinusitis Clinical Trials

Effects of Anti-IgE Antibody Omalizumab on Patients With Chronic Sinusitis

Start date: January 2008
Phase: Phase 4
Study type: Interventional

We propose to study the effects of Xolair on patients with chronic sinusitis with or without nasal polyps. Because of the similarities between the inflammatory processes found in asthmas and rhinitis to those found in chronic sinusitis, we hypothesize that sinusitis should respond to Xolair, just as asthma.