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Otorrhea clinical trials

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NCT ID: NCT04807660 Recruiting - Otorrhea Clinical Trials

Bacteriological Evaluation of Children With Otorrhea

Start date: October 1, 2015
Phase:
Study type: Observational

After pneumococcal conjugate vaccine implementation, the number of acute otitis media (AOM) episodes has decreased, but AOM still remains among the most common diagnoses in childhood. From 2% to 17% of cases of AOM feature spontaneous perforation of the tympanic membrane (SPTM). The aim of this study was to describe the bacteriological causes of SPTM several years after PCV13 implementation, in 2010.

NCT ID: NCT03347461 Withdrawn - Clinical trials for Otitis Media With Effusion in Children

Otiprio Versus Ciprodex Tympanostomy Tube Outcomes

Start date: October 2018
Phase: Phase 4
Study type: Interventional

Otolaryngologists routinely administer ear drops at the time of tympanostomy tube placement in order to prevent tube otorrhea; however, there is a lack of consensus as to which drops are the most effective, and whether a post-operative regimen should be used. Utilizing drops postoperatively places the onus of administration on parents who may have various difficulties in delivering the drops to their child's ears. Additionally, prescribing drops postoperatively is a health care cost. The purpose of this study is to determine if there is a difference in prevention of tympanostomy tube failure (defined as tube blockage or otorrhea) between Otiprio administered once intraoperatively, Ciprodex otic dropgs administered once intraoperatively, and Ciprodex otic drops administered intraoperatively with a postoperative course.

NCT ID: NCT02817347 Terminated - Otitis Media Clinical Trials

A Clinical Trial of YH1177 in Patients With Otitis Media and Otorrhea

Start date: June 2016
Phase: Phase 1/Phase 2
Study type: Interventional

In patients with otitis media presenting with otoscopy-confirmed otorrhea who had tympanostomy tube insertion or tympanic perforation, to evaluate the safety, tolerability, and the proportion of patients with cessation of otorrhea after ear-drop administration of YH1177 or YH1177-D for 14 days and therefore to determine the optimal clinical dose.

NCT ID: NCT01111877 Terminated - Otorrhea Clinical Trials

Natural History Study of Incidence of Otorrhea Following Tympanostomy Tube Insertion in Children 6 Months to 12 Years

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

This study was conducted to describe the time to first incidence of otorrhea post tympanostomy tube insertion.

NCT ID: NCT00956748 Withdrawn - Otitis Media Clinical Trials

N-Acetylcysteine as an Adjunct for Refractory Chronic Suppurative Otitis Media

Start date: November 29, 2019
Phase: Phase 4
Study type: Interventional

Chronic suppurative otitis media (CSOM) can be particularly difficult to treat as a number of patients do not respond to routine antibiotic or surgical treatments. The current treatment involves administering combination antibiotic anti-inflammatory ear drops such as Ciprodex (ciprofloxacin 0.3% / dexamethasone 0.1%). Although most patients experience a relief of symptoms, a fraction of patients remain refractory to treatment. Recent findings suggest that the addition of N-acetylcysteine (0.5-2%) to Ciprodex is a superior treatment for otitis media with effusion compared to the use of Ciprodex alone.