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Gamma Knife Radiosurgery vs Initial Conservative Treatment for Vestibular Schwannoma Patients With Preserved Hearing, a Prospective Randomized Study

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Karolinska Institute

Status

Completed

Conditions

Vestibular Schwannoma

Treatments

Radiation: Initial Gamma knife radiosurgery

Study type

Interventional

Funder types

Other

Identifiers

NCT01938677
2013/211-31/1

Details and patient eligibility

About

The effect of Gamma knife radiosurgery (GKRS) on hearing loss, in patients with vestibular schwannoma (VS) and preserved hearing is still unclear. Retrospective data indicate that the hearing is preserved in most patient years after the gamma knife treatment. Recent prospective data suggests that radiosurgery could be a hearing preserving treatment for these patients.

The main objective of this study is to evaluate if GKRS can inhibit progression of hearing loss in patients with VS. Patients with preserved hearing will be offered to participate in the study and randomized ether to GKRS or initial conservative treatment for their vestibular schwannoma. They will then be followed with scheduled magnetic resonance image(MRI) and audiometry and evaluated after one, three and five years after treatment.

Enrollment

67 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients newly (<6 months) diagnosed with Vestibular schwannoma less than 20 mm in diameter.

  2. Vestibular schwannoma with or without evidence of growth.

  3. Patients between 18 and 80 years of age.

  4. Karnofsky performance score >70

  5. Patients with vestibular schwannoma and preserved hearing according to Gardner Robertson class 1-2, and speech discrimination (SD) scores between 50-100% will participate in the hearing preservation part of the study.

Exclusion criteria

    1. Patients with Neurofibromatosis type 2 will be excluded to achieve a homogenous study population.

    2. Patients who had other treatments prior to the GKRS (usually microsurgery (MS), GKRS or external beam radiation) for their tumour will also be excluded for the same reason.

    3. Patients who are not citizens in the country where they will be followed will be excluded, to reassure the same follow up within the study population.

    4. Hearing loss due injury or to active ear disease, such as Meniere´s disease, otosclerosis or chronic otitis media.

    5. Patients with poor comprehension of the the language in the country where they are followed, such that adequate performance on speech tests, are unlikely.

    6. Claustrophobia, making MR follow up impossible without sedation. 7. Alcohol- or narcotic abuses that effect compliance to the follow up. 8. Uncontrolled neoplastic disease.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

67 participants in 2 patient groups

Initial Gamma knife
Experimental group
Description:
Patients with VS and preserved hearing, randomized to initial gamma knife radiosurgery will receive this treatment within a few months after enrollment
Treatment:
Radiation: Initial Gamma knife radiosurgery
Initial conservative
No Intervention group
Description:
Patients with VS and preserved hearing, randomized to initial conservative treatment will initially be followed with repeated MRI and audiometry. If MRI show progression of VS requiring intervention, patients will receive treatment but still belong to the initial treatment arm, according to intention to treat.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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