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Hearing Loss, Sudden clinical trials

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NCT ID: NCT04902963 Completed - Clinical trials for Eustachian Tube Dysfunction

What is the Tympanic Membrane Healing Time After Insertion of a Gelfoam PE Tube?

Start date: March 15, 2011
Phase: N/A
Study type: Interventional

Pilot study done to evaluate the breakdown and and potential utility of a bioabsorbable ventilation ear tube made with gelatin.

NCT ID: NCT04766853 Recruiting - Meniere Disease Clinical Trials

Verification of the Efficacy/Safety of the Intratympanic Drug Delivery for Hearing Loss

Start date: July 22, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

This study is a prospective, randomized pilot study. To verify an efficacy and safety of the Intratympanic drug delivery vehicle, patients who have not responded to the existing standard treatment will be enrolled. Hearing test, endoscopy of tympanic membrane and CT scans will be conducted after intratympanic treatment for evaluation.

NCT ID: NCT04629664 Completed - Clinical trials for Hearing Loss, Sensorineural

FX-322 in Adults With Severe Sensorineural Hearing Loss

Start date: November 2, 2020
Phase: Phase 1
Study type: Interventional

This is a Phase 1b, prospective, randomized, double-blind, placebo-controlled, single-dose, multicenter, safety study of FX-322, administered by intratympanic injection, in adults with severe sensorineural hearing loss.

NCT ID: NCT04601909 Completed - Clinical trials for Hearing Loss, Sensorineural

FX-322 in Adults With Age-Related Sensorineural Hearing Loss

Start date: September 17, 2020
Phase: Phase 1
Study type: Interventional

This is a Phase 1b, prospective, randomized, double-blind, placebo-controlled, single-dose, multicenter, safety study of FX-322, administered by intratympanic injection, in adults with age-related sensorineural hearing loss.

NCT ID: NCT04449848 Not yet recruiting - Sudden Hearing Loss Clinical Trials

The Effect of Patient's Position After Intra-tympanic Injection on the Amount of Fluid in the Middle Ear

Start date: August 1, 2020
Phase: N/A
Study type: Interventional

During the regular protocol of Intra-tympanic injections of Dexamethasone to the middle ear due to Sudden Sensorineural Hearing Loss, the patients will be sitted once after the injection instead of lying down. They will be then asked to rate their taste as a reference to the amount of fluid leaking to the throat through the eustachian tube.

NCT ID: NCT04384640 Not yet recruiting - Sudden Hearing Loss Clinical Trials

The Effect of Patient's Position After Intra-tympanic Injection

Start date: July 1, 2020
Phase:
Study type: Observational

The effect of the patient's head on the leakage of steroids from the middle ear to the throat will be studied. The patients will be seated after one of the intra tympanic injections that are routonely performed due to Sudden Sensorineural Hearin Loss (SNHL). The patients will be asked if they taste the steroids in their throats.

NCT ID: NCT04192656 Recruiting - Clinical trials for Obstructive Sleep Apnea

The Effect of PAP on ISSHL Comorbided With OSA

Start date: November 1, 2019
Phase: Phase 4
Study type: Interventional

This clinical randomized controlled study is to explore the effect of positive airway pressure(PAP) on patients in Beijing Tsinghua Changgung Hospital diagnosed with both idiopathic sudden sensorineural hearing loss comorbided(ISSHL) and obstructive sleep apnea(OSA) between Dec. 2019 to Dec. 2029.

NCT ID: NCT04129983 Not yet recruiting - Clinical trials for Hearing Loss, Sudden

Treatment of Sudden Deafness With Prednisone+Hyperbaric Oxygen and Prednisone+Somatosensory Stimulation

Start date: June 2020
Phase: N/A
Study type: Interventional

To study the effective treatment of sudden deafness by giving prednisone, hyperbaric oxygen and somatosensory stimulation to sudden deafness patients.

NCT ID: NCT04129697 Not yet recruiting - Clinical trials for Dexamethasone or Methylprednisolone; Sudden Hearing Loss; Intratympanic Steroid

Intratympanic Steroids for Sudden Hearing Loss

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

For patients with sudden hearing loss, the initial treatment is not usually effective. We use Dexamethasone or Methylprednisolone to be an Intratympanic steroid administration as a salvage treatment. An randomized, double-blind, multi-center study is designed to find the difference between Dexamethasone or Methylprednisolone.

NCT ID: NCT03974867 Not yet recruiting - Sudden Hearing Loss Clinical Trials

Vestibular Prognosis Assessment of ISSNHL With Vestibular Dysfunction Treated With Oral or Intratympanic Glucocorticoids

Start date: July 2019
Phase: N/A
Study type: Interventional

Idiopathic sudden sensorineural hearing loss (ISSNHL) is a complicated hearing impairment with unclear etiology and unsatisfying treatment effects. Vestibular dysfunction like vertigo has been considered as a risk factor of profound hearing loss and poor prognosis in ISSNHL. Glucocorticoids, administered through oral or intratympanic way, is currently a regular and standard treatment for ISSNHL based on hearing outcome. However, little investigations have been conducted on recovery process and treatment effects of glucocorticoids on vestibular dysfunctions of ISSNHL. This study aims to evaluate the recovery pattern and possible process of vestibular system in ISSNHL with vestibular dysfunction, and to compare the efficacy of oral or intratympanic glucocorticoids in these participants. A randomized, outcome assessor- and statistical analyst-blinded, controlled, clinical trial will be carried out. 72 patients complaining of vestibular dysfunction appearing as vertigo, dizziness, imbalance or lateropulsion with ISSNHL will be recruited and randomized into two arms of oral or intratympanic glucocorticoids therapy in 1:1 allocation. The primary outcomes will be subjective feelings evaluated by duration of vestibular dysfunction symptoms, dizziness-related handicap, visual analogue scale for vertigo, and objective vestibular function tests results assessed by sensory organization test, caloric test, video head impulse test and vestibular evoked myogenic potentials. Assessment will be performed at baseline and at 1, 2, 4, and 8 weeks post-randomization.