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Otitis clinical trials

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NCT ID: NCT03768635 Completed - Clinical trials for Bone and Joint Infection

Necrotizing External Otitis : Study in a Regional Bone and Joint Infection Reference Center

Start date: January 1, 2006
Phase:
Study type: Observational

The malignant external otitis is a rare disease which arises more frequently at the elderly and the diabetics patients. To our knowledge, there are few data and it is not wellc known byclinicians. Nevertheless it exposes to neurological complications potentially serious and crippling.

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.

NCT ID: NCT03503591 Completed - Otitis Media Clinical Trials

Study of the Hummingbird TTS™ Tympanostomy Tube System

Start date: January 29, 2016
Phase:
Study type: Observational

The objective of this study was continued commercial evaluation of the intraoperative safety and performance of the H-TTS for the placement of ventilation tubes in pediatric patients undergoing a tympanostomy procedure under moderate sedation and local anesthetic.

NCT ID: NCT03398044 Completed - Hearing Loss Clinical Trials

Administration of Dexamethasone in PONV Prophylaxis in Children Undergoing Adenotomy

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Adenotomy, together with tonsillectomy, belongs among the most frequently performed surgical procedures in paediatric patients. These surgical procedures are associated with the second highest incidence of post-operative nausea and vomiting (PONV) (following strabism correction surgery) in paediatric surgery. PONV is associated, apart from the discomfort for the child, with a number of complications: dehydration, metabolic disruption or danger of haemorrhage and aspiration of the gastric content. Adenotomy is a typologically completely different surgical procedure, with a different target structure of the surgery, and the length and invasiveness of the procedure. Thus, it is possible to expect a difference in PONV incidence when compared to tonsillectomy. Adenotomy is a surgical procedure performed namely in children of the pre-school age. This is associated, among others, also with the problem of objectivization of post-operative nausea, which is very difficult to verbalize in small children, being a subjective feeling of body discomfort. It is possible to expect that the overall incidence of PONV will be significantly underestimated.

NCT ID: NCT03323736 Completed - Clinical trials for AOM - Acute Otitis Media

In-Office Tympanostomy Tube Placement in Children (OTTER)

OTTER
Start date: October 31, 2017
Phase: Phase 3
Study type: Interventional

A prospective, single-arm, multicenter study to evaluate effectiveness and safety of Tymbion iontophoresis and tympanostomy tube placement using the Tula Iontophoresis and Tube Delivery Systems for children in an office setting.