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Nasal Polyps clinical trials

View clinical trials related to Nasal Polyps.

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NCT ID: NCT02743871 Completed - Healthy Clinical Trials

Study Of PF-06817024 In Healthy Subjects, In Patients With Chronic Rhinosinusitis With Nasal Polyps And in Patients With Atopic Dermatitis

Start date: April 27, 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate safety, tolerability, pharmacokinetics, and pharmacodynamics of PF-06817024 in healthy volunteers, in participants with chronic rhinosinusitis, with nasal polyps and in participants with moderate-to-severe Atopic Dermatitis

NCT ID: NCT02734849 Completed - Nasal Polyposis Clinical Trials

Study to Evaluate Multiple Doses in Patients With Nasal Polyposis

Start date: April 2016
Phase: Phase 2
Study type: Interventional

This is a phase 2 study to evaluate multiple doses of AK001 across 2 active doses. Pharmacodynamic activity will also be evaluated.

NCT ID: NCT02562924 Completed - Chronic Sinusitis Clinical Trials

The Efficacy of MEDIHONEY® for Chronic Rhinosinusitis With Nasal Polyposis After Functional Endoscopic Sinus Surgery

Start date: November 2015
Phase: N/A
Study type: Interventional

This study will assess the effectiveness of MEDIHONEY® sinus rinses (alone or in combination with intranasal corticosteroids) vs. intranasal corticosteroid sinus rinses on mucosal healing and polyp recurrence in the post-operative period following functional endoscopic sinus surgery.

NCT ID: NCT02559284 Completed - Surgery Clinical Trials

RESPIMER® Netiflow® vs. Saline Solutions During Nasal Irrigation Following Bilateral Ethmoidectomy (Nasal Polyposis)

NETIFLOW
Start date: April 2015
Phase: N/A
Study type: Interventional

The main objective of this study is to compare the effects of RESPIMER® NetiFlow® solution and device versus saline solution (0.9% NaCl), the standard treatment, used with RESPIMER® NetiFlow® device, both used postoperative care, in the context of ethmoid sinus surgery, at 14 days post-surgery.

NCT ID: NCT02484859 Completed - Nasal Polyps Clinical Trials

Comparison of Metoprolol and Tramadol With Remifentanil in Endoscopic Sinus Surgery

Start date: July 2015
Phase: Phase 4
Study type: Interventional

Functional endoscopic sinus surgery (FESS) is indicated in diseases such as chronic sinusitis refractory to medical treatment, nasal polyposis, mass lesions in the nasal cavity. The purpose of this study is to determine whether tramadol and metoprolol are as effective as remifentanil in providing controlled hypotension during FESS.

NCT ID: NCT02476929 Completed - Allergic Rhinitis Clinical Trials

Detection and Use of Nasal Nitrous Oxide and the Electronic Nose

EPONA
Start date: January 2013
Phase: N/A
Study type: Interventional

Introduction: Rhinitis, sinonasal polyposis (SP) and asthma are diseases whose pathogenesis is based on inflammation. This will determine the presence of disease, its evolution and its treatment. It is therefore very important to develop and validate methodologies that allow us to noninvasively detect inflammation of the airways. Thus, just as exhaled nitric oxide (FeNO) has been studied as an important non-invasive marker of inflammation of the lower airways, nasal nitric oxide (nNO) may be a good marker of nasal inflammation. Furthermore, the electronic nose is an electronic nanosensor device capable of detecting specific volatile organic compounds (VOCs) that can be used as a non-invasive biomarker of biochemical processes in different diseases whose pathophysiology is also based on inflammation. Objective: To determine reference values of nNO and different patterns of VOCs in healthy individuals, individuals with allergic rhinitis (AR) and non-allergic rhinitis and individuals with SP and asthma. Methodology: Prospective, controlled study. Four groups will be included: Healthy subjects, patients with AR, non-allergic rhinitis and patients with SP and asthma (n=252). Prick-test to pneumoallergens will be performed. Determination of FeNO, nNO, lung function tests, measurement of VOCs by the electronic nose and blood samples will be taken. Bilateral nasal endoscopy and sample collection using the technique of brushing of mucosa and the placement of filter papers, for the study of nasal cytology and mediators of inflammation.

NCT ID: NCT02427503 Completed - Asthma Clinical Trials

ATP Project (Asthma afTer Polypectomy)

ATP
Start date: July 2016
Phase:
Study type: Observational [Patient Registry]

Inflammation of the nasal and bronchial mucosa characterizing rhinitis and asthma are probably manifestations of the same disease. Multiple functional observations, pathogenic and clinical support that assertion. It is noteworthy that most asthma patients, who underwent a nasal endoscopic polypectomy, improve your asthma after surgery. This improvement would be related to the administration of oral steroids that these patients usually receive after surgery, or the disappearance of nasal discomfort caused by nasal polyps to improve ventilation. But this does not explain why this improvement, in some cases lasting for months after the operation, and without receiving oral steroids. It is speculated that severe nasal inflammation due to nasal polyps stimulate the bone marrow to produce more eosinophils, an increased supply of blood eosinophils, and consequently, a major bronchial eosinophilic inflammation, aggravating asthma. However, it is noteworthy that studies have evaluated the clinical impact in asthma after endoscopic nasal polypectomy, are scarce or performed on a small number of cases, the results are inconsistent and do not allow categorically whether or not such positive association. And more importantly, none of them included measurements of airway inflammation and hypothesized relationship between bronchial eosinophilic inflammation and nasal polyposis, aclarar.La remains finding that provides nasal endoscopic polypectomy objective improvement of severe asthma it could be a future therapeutic option to consider in patients with asthma and rhinosinusal polyposis.

NCT ID: NCT02291549 Completed - Chronic Sinusitis Clinical Trials

S8 Sinus Implant in Chronic Sinusitis Patients With Recurrent Nasal Polyps

RESOLVE_II
Start date: December 2014
Phase: Phase 3
Study type: Interventional

The RESOLVE II Study is a randomized, single-blind, parallel arm, concurrently controlled, multicenter study with 300 chronic sinusitis patients who had prior endoscopic sinus surgery but present with recurrent sinus obstruction.

NCT ID: NCT02217332 Completed - Clinical trials for Chronic Sinusitis With Nasal Polyps and Eosinophilia

Study of Dexpramipexole Chronic Sinusitis With Nasal Polyps and Eosinophilia

CS201
Start date: August 2014
Phase: Phase 2
Study type: Interventional

Phase 2, open-label, multi-center study to evaluate the clinical effects of oral administration of dexpramipexole for 6 months in subjects with chronic sinusitis with nasal polyps and eosinophilia.

NCT ID: NCT02194062 Completed - Sinusitis Clinical Trials

Comparison of Nasal Steroids After FESS in CRSwNP

Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to compare intranasal fluticasone spray with budesonide nasal saline rinses in both the upright and head forward positions in patients who have had functional endoscopic sinus surgery (FESS) for chronic rhinosinusitis with nasal polyposis (CRSwNP) and measure differences in Sinonasal Outcome Test-22 (SNOT-22) scores and Lund- Kennedy scores on rigid nasal endoscopy at time points 1 week, 3 weeks, 6 weeks, 2 months, 4 months, and 6 months post-op.