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Recruiting NCT06844461

Quality of Life and Decisional Regret in Patients Affected by Acoustic Neuroma

Observational Quality of Life Outcomes Acoustic Schwannoma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Quality of Life Outcomes, Acoustic Schwannoma. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Italian translation and validation study of two different questionnaire (VSQOL and DRS) about quality of life in patient with acoustic schwannoma.

Primary outcome measures

  • VSQOL-It [Time frame: From the surgery to the enrollment time (6 months post-treatment) for surgical group. At baseline at enrollment for wait-and-scan group]
  • DRS-It [Time frame: From the surgery to the enrollment time (6 months post-treatment) for surgical group. At baseline at enrollment for wait-and-scan group]
Secondary outcome measures (2)
  • PANQOL [Time frame: From the surgery to the enrollment time (6 months post-treatment) for surgical group. At baseline at enrollment for wait-and-scan group]
  • DASS-21 Questionnaire [Time frame: From the surgery to the enrollment time (6 months post-treatment) for surgical group. At baseline at enrollment for wait-and-scan group]

Eligibility criteria

Inclusion criteria

  • Patient with sporadic acoustic neuroma in follow-up with wait and scan protocol or treated with microsurgical resection with any approach

Exclusion criteria

  • Patient with NF2
  • Patient previuosly treated with RT in the head and neck district
  • Patient with pre-treatment facial palsy ipsi and controlateral
  • Patient non native italian speakers
  • Patient with major mental illness already existing before the acoustic neuroma diagnosis
  • Patient with neurological issues such as chronic migraine or postural instability already existing before the acoustic neuroma diagnosis

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-control

Study locations

Italy · 1 center
  • Irccs Aou Bologna — Bologna

Identifiers

NCT: NCT06844461 · QOL-DR-NEUROMA

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗