Clinical Trials Logo

Otitis Media clinical trials

View clinical trials related to Otitis Media.

Filter by:
  • Not yet recruiting  
  • « Prev · Page 2

NCT ID: NCT03315156 Not yet recruiting - Acute Otitis Media Clinical Trials

Taste Changes in Acute Otitis Media

Start date: March 1, 2018
Phase: N/A
Study type: Observational

Detection of taste changes in Acute Otitis Media (AOM) patients.

NCT ID: NCT02549612 Not yet recruiting - Acute Otitis Media Clinical Trials

The Effect of Early Non-Surgical Treatment of Children With Middle Ear Effusion on the Hearing

Start date: March 2017
Phase: N/A
Study type: Interventional

Secretory otitis media (SOM) or middle ear effusion is a common finding after acute otitis media (AOM). It is usually associated with 5-15 deci Bells hearing loss. Although spontaneous resolution with normalisation of hearing is the usual outcome, this can take several months. Secretory otitis media is the most common cause of hearing impairment in the paediatric age group. When the hearing loss caused by SOM is bilateral and persists for 3-6 months or more, surgery with tympanostomy tube insertion under general anaesthesia is indicated. In Sweden, 10000 children undergo this operation annually. Although many children with unilateral or bilateral SOM improve in the summer, the problem usually recurs in the autumn or winter. The cost of SOM for the Swedish society was 600 million Swedish crowns 2005. In two previous studies, the investigators concluded that the nonsurgical treatment method, that was developed to assist children with SOM equalising their middle ear pressure, could normalise the hearing level in 80 % of children with SOM of minimum duration of 3 months. These children avoided therefore grommet insertion. The investigators would like to assess the effect of this new treatment method on hearing directly after AOM. The investigators expect that using the new method could rapidly normalise hearing in these cases and thereby operation with grommet insertion could be avoided.

NCT ID: NCT02477735 Not yet recruiting - Sleep Disturbances Clinical Trials

The Effect of Tympanostomy Tube Insertion on Sleep in Children With Chronic Otitis Media With Effusion

Start date: June 2015
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the prevalence of sleep disturbances in children with Chronic Otitis Media with Effusion (COME) and the effect of tympanostomy tube insertion (TTI) on sleep disturbances.

NCT ID: NCT01967498 Not yet recruiting - Clinical trials for Conductive Hearing Loss

Montelukast for Children With Chronic Otitis Media With Effusion (COME): A Double-blind, Placebo-controlled Study

COME
Start date: November 2013
Phase: N/A
Study type: Interventional

The purpose of our double-blind, placebo controlled study is to test the hypothesis that montelukast therapy might be associated with improved hearing in certain sub populations of children suffering from OME.

NCT ID: NCT01421199 Not yet recruiting - Clinical trials for Otitis Media With Effusion

Device Study to Evaluate the Detection and Characterization of Middle Ear Fluid in Children

Start date: September 2011
Phase: N/A
Study type: Interventional

The study has three objectives: 1. To determine if the device can detect if middle ear fluid is present in children who are scheduled for tube placement (myringotomy) 2. If fluid is present to characterize the fluid as thick or thin 3. Evaluate the safety of the device

NCT ID: NCT01157910 Not yet recruiting - Clinical trials for Chronic Otitis Media

Bacterial Assessment of Middle Ear Fluid in Children Undergoing Ventilation Tube Placement Surgery

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

Children with chronic otitis media have more resistant bacteria that require surgical intervention to eradicate the infections. The study will evaluate the dominant bacteria and their sensitivities to antibiotics. The information will assist in better treatment plans for children with chronic infections. The data will also assess the changing patterns in the bacteria colonizing middle ear fluid.

NCT ID: NCT00794105 Not yet recruiting - Otitis Media Ears. Clinical Trials

Observation of Gas Exchange in the Middle Ear

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

Observation of fluid behavior over a perforated eardrum. A comparison of the behavior of the gas in normal vs. different kinds of otitis media ears.

NCT ID: NCT00310349 Not yet recruiting - Clinical trials for Pneumococcal Infections

PneuMum: Pneumococcal Vaccination of Australian Indigenous Mothers to See if it Protects Their Babies From Ear Disease

Start date: March 2006
Phase: Phase 3
Study type: Interventional

PneuMum is a randomised controlled trial that aims to find out if pneumococcal vaccination for Australian Indigenous mothers, in the last few months of pregnancy or at delivery, can prevent ear disease in infants. Mothers will receive the 23 valent pneumococcal polysaccharide vaccine (23vPPV) either: a) during the third trimester of pregnancy; b) soon after child birth; or c) seven months after child birth (control group). The adult diphtheria, tetanus and acellular pertussis vaccine (dTPa) will be used as the control vaccine for the birth dose. The study aims to recruit 210 Indigenous women aged 18-39 years who have an uncomplicated pregnancy. Following recruitment, subjects will be randomly assigned to one of the three groups. Each mother and infant will be followed from pregnancy until the baby is seven months of age. Children will receive all of their routinely recommended vaccinations in accordance with the standard vaccination schedule. The primary outcome will be prevalence of ear infection at seven months of age, defined as middle ear effusion or tympanic membrane perforation or acute otitis media. Pneumatic otoscopy, video-otoscopy and tympanometry will be used in the ear examinations. The primary analyses will be a direct comparison of the proportion of infants in the control group who have nasopharyngeal carriage of vaccine type pneumococci at seven months of age compared to infants in each of the other two groups and a similar comparison of the proportion with middle ear disease.

NCT ID: NCT00248391 Not yet recruiting - Dental Caries Clinical Trials

The Influence of Feeding Position on Pulmonary Morbidity in Young Children

Start date: n/a
Phase: N/A
Study type: Interventional

Supine feeding position is associated with serous otitis media. The hypothesis is that supine feeding is associated with recurrent otitis media, tonsillar and adenoid hypertrophy and recurrent pneumonia secondary to recurrent aspiration.