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Otitis clinical trials

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NCT ID: NCT04395261 Completed - Clinical trials for Otitis Media With Effusion

Wideband Tympanometry in Otitis Media With Effusion

Start date: January 1, 2016
Phase:
Study type: Observational

The investigators asked the question if they can better estimate the middle ear status in OME that help them to decide between early intervention or longer follow up.

NCT ID: NCT04296448 Completed - Acute Otitis Media Clinical Trials

Evaluation of Cellphone Based Otoscopy in Pediatric Patients

Start date: September 1, 2019
Phase: N/A
Study type: Interventional

The Cellscope is an iPhone-based otoscope that uses the iPhone camera and light source to capture HIPAA compliant images and video recordings of the external and middle ear structure. This technology allows multiple providers, at different levels of training, the ability to simultaneously exam a child's external and middle ear structures. The investigators hypothesize this device will result in improved concordance in trainee/supervisor exam findings, increase trainee confidence in exam findings, decreased antibiotic prescriptions, and fewer repeat exams by multiple providers. Thus, this study has the potential to improve physician training and examination confidence, decrease the unnecessary use of antibiotics, and improve the patient/caregiver experience in healthcare interactions.

NCT ID: NCT04281901 Completed - Temporal Bone Clinical Trials

Efficacy of Platelet- and Extracellular Vesicle-rich Plasma in Chronic Postsurgical Temporal Bone Inflammations

PvRP-ear
Start date: March 20, 2019
Phase: N/A
Study type: Interventional

This clinical study evaluates the efficacy of the autologous blood-derived product called platelet- and extracellular vesicle-rich plasma (PVRP) for the treatment of chronically inflamed post-surgical temporal bone cavities. Half of the participants will be treated with platelet- and extracellular vesicle-rich plasma and another half with standard nonsurgical measures.

NCT ID: NCT04219553 Completed - Otitis Media Clinical Trials

Antimicrobial Stewardship in Community Pharmacy

Start date: May 25, 2017
Phase: N/A
Study type: Interventional

Acute otitis media (AOM) is the most common indication for antibiotics for Canadian paediatric patients. As the gatekeepers of safe and effective prescription pharmacotherapy, community pharmacists are well positioned to influence and optimize antibiotic use. The purpose of this project is to develop, implement, and evaluate an antimicrobial stewardship program in the community pharmacy setting that aims to optimize antibiotic use for AOM. This nonrandomized pre-post study includes children aged 6 months to 12 years presenting with an antibiotic prescription for AOM at two community pharmacies in Toronto, Ontario. Participants are excluded if they exhibit signs/symptoms of mastoiditis, have an additional indication for systemic antibiotics, or parents/guardians cannot consent in English. The multifaceted AMS intervention includes pharmacist education, a clinical decision support tool, a parent/guardian questionnaire, and individualized monthly audit and feedback with each pharmacist. Prescriptions are reviewed and adapted by the pharmacist to optimize congruence with 2016 Canadian Paediatric Society AOM guidelines. The primary outcome is the percentage change in guideline congruence attributable to pharmacist intervention. This study will provide insight into the opportunities and barriers of developing large-scale antimicrobial stewardship programs for community pharmacies.

NCT ID: NCT04016051 Completed - Otitis Media Clinical Trials

Acceptance of Clarithromycin in a Straw Compared to Syrup in Children With Upper Respiratory Tract Infections

DoSe iT
Start date: September 22, 2004
Phase: Phase 3
Study type: Interventional

This study was performed in children with upper respiratory tract infections (acute ear infection, infection of the tonsils or throat, or bacterial inflammation of the bronchi) who needed treatment with an antibiotic (clarithromycin). The study investigated a new technology which delivers the antibiotic in a straw (dose sipping technology, DST) in comparison to a marketed syrup.

NCT ID: NCT03975842 Completed - Clinical trials for Chronic Rhinosinusitis With Nasal Polyposis (CRSwNP)

Chronic Otitis Media With Effusion in Chronic Sinusitis With Polyps

Start date: January 2010
Phase:
Study type: Observational

The relationship between otitis media with effusion (OME) and chronic rhinosinusitis with nasal polyposis (CRSwNP) remains unclear. A cross-sectional study of 80 consecutively presenting patients who were diagnosed with CRSwNP was conducted. The aim was to ascertain the prevalence of OME in CRSwNP patients, to determine whether the severity of CRSwNP affected OME, and to identify risk factors for OME in CRSwNP patients.

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.