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Otitis Media clinical trials

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NCT ID: NCT03890107 Completed - Otitis Media Clinical Trials

Clinical Evaluation of the OtoSight

Start date: April 15, 2019
Phase:
Study type: Observational

The objective of this study is to evaluate the imaging capabilities and image analysis performance of the OtoSight Middle Ear Scope in pediatric patients undergoing tympanostomy tube placement for otitis media. In this observational study, results of OtoSight imaging will not affect patient standard of care.

NCT ID: NCT03864055 Completed - Otitis Media Clinical Trials

Otogenic CSVT Retrospective Case Series and Associated Thrombophilia

CSVT PCR
Start date: December 2, 2018
Phase:
Study type: Observational

The aim of this study is to report the clinical presentation, Microbiological, laboratory and imaging evaluation, prothrombotic factors analysis, medical and surgical management and outcomes in children with Otogenic Cerebral Sinus Vein Thrombosis (CSVT).

NCT ID: NCT03848026 Completed - Clinical trials for OTITIS MEDIA WITH EFFUSION

Tympanostomy Tube Extrusion Time & Viscosity

Start date: January 15, 2018
Phase:
Study type: Observational [Patient Registry]

Studies have focused on the factors that influence tympanostomy tube (TT) extrusion may contribute to the management of OME. In this study the investigators aimed to assess the correlation between the TT extrusion time and viscosity of the middle ear fluid. 33 patients scheduled for TT insertion included in the study. During the paracentesis, fluid from the middle ear was obtained, and the viscosity was measured with a viscometer. After the surgery, patients were controlled monthly until the tubes were seen extruded.The analysis of the correlation between tube extrusion time and viscosity was insignificant (p >0.05).

NCT ID: NCT03818815 Completed - Acute Otitis Media Clinical Trials

A Study to Assess the Safety, Tolerability and Efficacy of OP0201 as an Adjunct Treatment for Acute Otitis Media in Infants and Children Aged 6 to 24 Months

Start date: February 21, 2019
Phase: Phase 2
Study type: Interventional

The purpose of this study is to develop a better understanding of the safety, tolerability and efficacy of intranasal OP0201 as an adjunct treatment to oral antibiotics for the treatment of Acute Otitis Media (AOM) in infants and children.

NCT ID: NCT03766373 Completed - Acute Otitis Media Clinical Trials

Evaluation of Safety and Reduction of Ear Pain in Adults With Acute Otitis Media and Reduction of Ear Pain in Adults With Acute Otitis Media

Start date: January 7, 2019
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the Safety and Reduction of Ear Pain in Adults with Acute Otitis Media.

NCT ID: NCT03614117 Completed - Acute Otitis Media Clinical Trials

Effect of a New Probiotic Strain on Recurrent Acute Otitis Media in Children (PROMAR)

PROMAR
Start date: October 2, 2018
Phase: N/A
Study type: Interventional

An interventional, randomized, double-blind, placebo-controlled study will be conducted to investigate the effect of a new probiotic strain Lactobacillus salivarius PS7 on Acute Otitis Media (AOM) in children with recurrent AOM history. The study duration will be 7 months, which includes a 6-month product administration and a 1-month follow-up period. Participants will be randomized assigned to one of the three study groups: the control group; a 3 months probiotic +3 months placebo consumption group and a 6 months probiotic consumption group. The efficacy of the probiotic strain to reduce the incidence of AOM episodes will be assessed by counting AOM episodes occurring in study participants, during the entire intervention and follow-up periods, by bilateral comparison of each of the treatment groups with the control group according to the following hypothesis: "The number of AOM episodes occurring in participants who take the probiotic is the same as that for the participants in the control group. λc = λe". Where λc is the mean incidence of AOM in the control group and λe is the mean incidence of AOM in the groups taking the probiotic strain Lactobacillus salivarius PS7 obtained with 95% confidence interval.

NCT ID: NCT03611842 Completed - Clinical trials for Otitis Media With Effusion

Study of the Expression of MMPs in OME in Children With Atrophy of the Eardrum

MMP and OME
Start date: September 30, 2018
Phase:
Study type: Observational

Metalloproteinases (MMPs) constitute a family of endopeptidases that cleaves the extracellular matrix as collagen included in the eardrum. Activity of MMP has been shown in some otitis media with effusion (OME) fluids. These enzymes could be directly linked to the prosnostic of OME as it may damage the eardrum and leads to tympanic atrophy. The main goal of the study is to find out the correlation between activity of MMPs and tympanic atrophy. The investigator will also study if there is any clinical predictive factors in relation to the level of MMPs.

NCT ID: NCT03590912 Completed - Clinical trials for Otitis Media With Effusion

Efficacy and Cost Analysis of Steroids in Treatment of Otitis Media With Effusion

Start date: September 5, 2018
Phase: Phase 4
Study type: Interventional

We intend to study the cost of treatment, efficacy and adverse effects for Otitis media with effusion.

NCT ID: NCT03556215 Completed - Clinical trials for Chronic Recurrent Otitis Media

Balloon Eustachian Tuboplasty in Treatment of Chronic Eustachian Tube Dysfunction

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

The prevalence of Eustachian tube (ET) dysfunction in adults reaches 1%. It causes a feeling of fullness in the ear, otalgia and hearing loss and can lead to recurrent acute otitis media, development of chronic otitis media with effusion and cholesteatoma. Endoscopic transnasal balloon ET dilatation is a novel surgical technique for ET dysfunction. The main goal is to restore ET function by dilation its cartilaginous part leading to better ventilation and drainage of the middle ear. However, its real effect in the treatment of particular subgroups of patients with ET dysfunction remains unknown. Patients are mostly evaluated as one group. Adults with chronic ET dysfunction will be strictly divided into particular subgroups and included in the study. Subgroups will be compared in order to identify treatment effect in particular subgroups.

NCT ID: NCT03544138 Completed - Otitis Media Clinical Trials

In-Office Study of the Hummingbird® in Children 6 Months-21 Years Old

Start date: July 24, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the safety and performance of the Hummingbird® for the placement of ear tubes in children undergoing tympanostomy tube placement in an otolaryngology clinic using local anesthetic.