Hearing Loss Clinical Trials

A listing of Hearing Loss medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

Filter By
Clear all Advanced
I am/have/had
added new label for I am/have/had
more
I am looking for
added new label for I am looking for
more
Advanced Filters
Found 210 clinical trials
Establishment and Application of a New Imaging System for Otology Based on Ultra-high Resolution CT

Tinnitus, hearing loss and vertigo are the three major diseases of otology, affecting hundreds of millions of people in our country, and are major health problems. Ear structures and lesions are

peripheral vertigo
audiogram
hard of hearing
tinnitus
deafness
  • 0 views
  • 07 Oct, 2022
  • 1 location
Investigation of Anatomical Correlates of Speech Discrimination

Understanding speech is essential for good communication. Individuals with hearing loss and poor speech discrimination often have little success with hearing aids because amplifying sound

hard of hearing
sensorineural hearing loss
Accepts healthy volunteers
audiogram
fitting
  • 240 views
  • 22 Jan, 2022
  • 1 location
BBD Longitudinal Study of Osteogenesis Imperfecta

Osteogenesis Imperfecta (OI) is a rare disorder of increased bone fragility characterized by fractures with minimal or absent trauma, dentinogenesis imperfecta (DI), and, in adult years, hearing

bone disease
hearing loss
dentinogenesis imperfecta
col1a1
short stature
  • 113 views
  • 26 Mar, 2022
  • 12 locations
Swiss Austrian German Testicular Cancer Cohort Study - SAG TCCS

document long-term toxicities of the treatment (cardiovascular, gonadal, hearing impairment, renal function and second malignancies) and psychosocial aspects. This cohort study will determine the relevance

metastasis
cardiovascular disease
renal function tests
seminoma
  • 76 views
  • 09 Aug, 2021
  • 1 location
Genetic Analysis to Predict the Development of Paget's Disease (GAPDPD)

Paget's disease of the bone (PDB) is a skeletal disorder with a strong genetic component which can be associated with various complications such as pain, bone deformity, arthritis and deafness

blood test
Accepts healthy volunteers
  • 0 views
  • 16 May, 2022
  • 1 location
The Natural History of GATA2 Deficiency and Related Disorders

develop few problems from it. Others can have a wide range of health problems, from skin problems, to hearing loss, to cancer. These problems can happen at any age. Researchers want to study GATA2

cancer
Accepts healthy volunteers
  • 34 views
  • 24 Oct, 2022
  • 1 location
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford (CoRDS)

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures …

other disease
rare diseases
  • 4 views
  • 15 Jul, 2022
  • 2 locations
Genotype-Phenotype Correlations in Patients With Alport Syndrome

Alport syndrome (AS) is caused by pathogenic variants in the type IV collagen genes COL4A3, COL4A4, and COL4A5. This study aims to enroll families and patients with a history of renal hematuria in 27 hospitals and detect these three genes for AS screening. This study also aims to analysis the …

  • 0 views
  • 11 Jul, 2021
  • 1 location
North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC) (NAMDC)

The North American Mitochondrial Disease Consortium (NAMDC) maintains a patient contact registry and tissue biorepository for patients with mitochondrial disorders.

mitochondrial dna
Accepts healthy volunteers
  • 44 views
  • 04 Oct, 2022
  • 17 locations
International Primary Ciliary Dyskinesia Cohort (iPCD)

The iPCD Cohort is a retrospective international cohort that assembles available datasets with clinical and diagnostic data from patients suffering from primary ciliary dyskinesia (PCD) worldwide, to answer pertinent questions on clinical phenotype, disease severity, prognosis and effect of treatments in patients with this rare multiorgan disease.

  • 53 views
  • 03 Mar, 2022
  • 1 location