Autologous Bone Marrow Harvest and Transplant for Sensorineural Hearing Loss

J

James Baumgartner, MD

Status and phase

Suspended
Phase 2
Phase 1

Conditions

Sensorineural Hearing Loss

Treatments

Genetic: Autologous Bone Marrow Infusion

Study type

Interventional

Funder types

Other

Identifiers

NCT02616172
695389

Details and patient eligibility

About

Autologous human bone marrow mononuclear fraction (BMMF) will be harvested and given to children with bilateral moderate to severe sensorineural hearing loss. The aim is to determine if bone marrow mononuclear fraction (BMMF) infusion is safe, feasible, improves inner ear function, audition, and language development.

Full description

Autologous human bone marrow mononuclear fraction (BMMF) will be given to children with bilateral moderate to severe sensorineural hearing loss. Subjects will come to Orlando for pretesting to include an Magnetic Resonance Imaging (MRI), Auditory brainstem response (ABR), blood work: Complete metabolic panel (CMP), Complete blood count (CBC), Hepatic Function Panel, Prothrombin (PT), Partial thromboplastin time (PTT), International normalized ration (INR), Chest Xray, and a Speech and Language Evaluation. After pretesting, the subjects will undergo a bone marrow harvest and then receive their autologous bone marrow mononuclear fraction (BMMF) intravenously. The subjects will then be monitored for 24 hours post infusion. After 24 hours, the subject will undergo repeat blood work and a chest x ray. Subjects will then be discharged home. Subjects will follow up in Orlando at 1 month, 6 months and 1 year post infusion. Follow up testing will repeat the exams performed at pretesting.

Enrollment

10 estimated patients

Sex

All

Ages

2 to 6 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Evidence of sensorineural hearing loss that is,

  • Bilaterally Moderate or Profound in degree
  • Symmetrical or asymmetrical configuration
  • Sudden or progressive in presentation
  • Normally shaped cochlea, as determined by Magnetic Resonance Imaging or computed tomography (CT)

The loss must be considered:

  • Acquired
  • Unknown with genetic testing negative. (Genetic testing is not required for Cytomegalovirus (CMV) positive children due to Cytomegalovirus (CMV) known to be number one cause of hearing loss)
  • Fitted for hearing aids no later than six months post detection of loss unless not recommended by treating audiologist or physicians
  • Enrollment in a parent/child intervention program
  • Age 2 years - 6 years old at time of infusion with 2 to 4 years of time elapsed since diagnosis of hearing loss at the time of bone marrow mononuclear fraction (BMMF) infusion.
  • Ability of the child and caregiver to travel to Orlando, and stay for at least 4 days, and to return for all follow-up visits.

Exclusion criteria

Inability to obtain all pertinent medical records:

(pertinent physician notes, speech language pathology notes, laboratory findings, test results and imaging studies-must be sent to the research team at least prior to the subject arriving at the study location for preliminary screening and eligibility assessment, preferably14 days before the scheduled visit.)

Known history of:

  • Recently treated (ear or any infections) infection less than 2 weeks before infusion.
  • Renal disease of altered renal function as defined by serum creatinine > 1.5 mg/dl at admission.
  • Hepatic disease or altered liver function as defined by Alanine Transaminase (SGPT) > 150 U/L, and or Total Bilirubin > 1.3 mg/dL
  • Malignancy
  • Immunosuppression as defined by White Blood Cell (WBC) < 3,000 at admission
  • Human Immunodeficiency Virus (HIV)
  • Hepatitis B
  • Hepatitis C
  • Pneumonia, or chronic lung disease requiring oxygen
  • Any evidence of active maternal infection during the pregnancy
  • Participation in a concurrent intervention study
  • Mild hearing loss with no evidence of moderate of severe loss
  • Unwillingness or inability to stay for 4 days following infusion (should problems arise following the infusion) and to return for the one month, six month and one year follow-up visits.
  • Evidence of conductive hearing loss
  • Documented recurrent middle ear infections which are frequent (>5 per year)
  • Otitis media at the time of examination
  • Before 2 years from identification of hearing loss at time of infusion
  • After 4 years from identification of hearing loss at time of infusion

Diagnosis of the following syndromic cause for hearing loss

  • CHARGE
  • Waardenburg
  • Brachio-Oto-Renal
  • Pendred
  • Alport
  • Treacher-Collins
  • Usher
  • Stickler Syndrome

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Autologous bone marrow infusion
Experimental group
Description:
One time administration of autologous bone marrow mononuclear cells intravenously, minimum dose of 6 million cells per kg Total nucleated cells.
Treatment:
Genetic: Autologous Bone Marrow Infusion

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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