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Nasal Obstruction clinical trials

View clinical trials related to Nasal Obstruction.

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NCT ID: NCT01702103 Not yet recruiting - Nasal Obstruction Clinical Trials

Demonstrate the Therapeutic Clinical Equivalence of Two Mometasone Nasal Sprays

PHT-01-12
Start date: October 2012
Phase: Phase 3
Study type: Interventional

Demonstrate the therapeutic clinical equivalence of two mometasone nasal sprays in the relief of the signs and symptoms of perennial allergic rhinitis, in term of changes at week 8 from baseline of Total Nasal Symptom Scores (TNSS).

NCT ID: NCT01695967 Completed - Sleep Apnea Clinical Trials

Turbinate Cauterization in Pediatric Patients With Nasal Obstruction

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

patients will be placed in 2 groups, with or without turbinate cautery ( a surgical method to reduce the size of the skin covered bones in the nose), at the time of adenoidectomy and tonsillectomy. It will compare the amount of nasal congestion for each group with the idea that it will be less if treated with turbinate cauterization. Assessments from baseline to 6 months post procedure will be compared between the two groups.

NCT ID: NCT01541839 Completed - Nasal Obstruction Clinical Trials

Comparison of a Septal Stapler to Suture Closure in Nasal Septoplasty

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

The primary objective of this study is to determine if there is a time savings in the operating room by using a septal stapler instead of suture in closure of primary septoplasty. The secondary objectives are to determine the subjective outcome of patients undergoing closure with the septal stapler instead of suture via questionnaire, and to determine if there is a difference in postoperative complications between groups.

NCT ID: NCT01506583 Completed - Fatigue Clinical Trials

Clinical Evaluation of QFlu Combo Test

QFlu
Start date: November 1, 2010
Phase:
Study type: Observational

Currently effective antivials for influenza treatment are two influenza viral neuraminidase inhibitors, oseltamivir (Tamiflu) and zanamivir (Relenza). Resistance to these drugs is reflected by reduced susceptibility of viral neuraminidase to these drugs. The hypothesis is that the signal ratio of two reagents (with or without a single concentration of the drug) correlates the IC50 value, an accurate measurement of drug resistance but impractical for clinical use.

NCT ID: NCT01457638 Completed - Quality of Life Clinical Trials

Inferior Turbinate Surgery in Rhinoseptoplasty: a Randomized Clinical Trial With Quality of Life Outcomes

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

The purpose of this study is to determine whether inferior turbinate surgery during rhinoseptoplasty is effective in improving quality of life and acoustic rhinometry outcomes.

NCT ID: NCT01411969 Completed - Nasal Obstruction Clinical Trials

Impact of External Nasal Dilator on the Rhinogram

ARENDS
Start date: June 2010
Phase: N/A
Study type: Observational

The aim of this study is to present new data for a better understanding of the anatomic correlation of these two notches. This study included 32 nasal cavities (16 individuals) with external nasal dilator strip (Breath Right®) and after decongestion (0.05% oxymetazoline chloride applied as an aerosol spray);

NCT ID: NCT01282125 Completed - Nasal Obstruction Clinical Trials

Nasal Obstruction in Sleep Apnea Patients Compared to the General Population

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

Recent clinical findings of research at Trondheim University Hospital suggest that surgical correction of the nose septum in addition to volume reduction of the nose cavity may be beneficial in patients who suffer from both nose obstruction and obstructive sleep apnea syndrome(data not yet published). This study aims to compare nose obstruction prevalence in sleep apnea patients and the general population

NCT ID: NCT01248325 Not yet recruiting - Sinusitis Clinical Trials

A Study of Luffa Operculate Nasal Solution 5mg/mL Compared With Saline (NaCl 09%) for the Relief of Nasal Obstruction

Start date: January 2011
Phase: Phase 3
Study type: Interventional

Sixty subjects will take part in this study. The subjects will be randomly assigned in a 1:1 ratio between the two arms of study. (Group A: Solution of Luffa Nasal Operculate 5mg/mL, Group B: saline). The subjects will use the study medication or comparative, according to their randomization, for a treatment period of 3 to 7 days. A follow-up visit will be made 15 days after initiation of treatment.

NCT ID: NCT00850876 Completed - Clinical trials for Obstructive Sleep Apnea Syndrome

Heated Humidified Continuous Positive Airway Pressure and Nasal Physiology

Start date: September 2008
Phase: N/A
Study type: Observational

Nasal continuous positive airway pressure can cause nasal side effects which can compromise compliance to therapy. Humidifiers can attenuate this effect. However, the mechanism by which humidified CPAP alleviates nasal symptoms has never been assessed objectively in OSA patients. Therefore, the purpose of this study is to examine the effect of humidified CPAP on nasal airway physiology with combined measurements of nasal resistance and level of inflammatory markers. The investigators' hypothesis is that the addition of heated humidification in CPAP decreases nasal airway resistance and nasal mucosal inflammation markers and thus, ameliorates nasal symptoms of OSAS patients.

NCT ID: NCT00793117 Completed - Pain Clinical Trials

The Effect of Packing in Post Operative Management of FESS

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

Chronic sinusitis is a very common problem. The functional endoscopic sinus surgery is a prevalent option to treat this disease.During usage of different techniques of surgery, the need for packing after surgery is debatable problem. So to solve this problem this research has been designed.