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NCT06954636Recruiting

Prognostic Potential of Olfactory Function in Glioblastoma: a Prospective Observational Study

Source: ClinicalTrials.gov · Last updated 24 Aug 2026

Brief summary (registry, in English)

The study aims to investigate the prognostic significance of olfactory function in patients with glioblastoma. We are examining olfactory function at various points during therapy and correlating the results with survival data. In addition, neurocognitive tests will be carried out to correlate the results of olfactory function with the patient's cognitive abilities. Investigations into the quality of life and psychological condition of the patients are also performed. In addition to the cohort of glioblastoma patients, there is a control cohort without tumor disease in which the olfactory testing is also carried out in order to have a comparison.

Status (registry)
Recruiting
Study type
Observational
Enrollment
128 (estimated)
First submitted
16 Apr 2025
Start date
3 May 2023
Primary completion date
31 Dec 2027
Lead sponsor
Sied Kebir
Diseases
Glioblastoma
NCT number
NCT06954636

What you commit to

  • Study type: Observational
  • Planned participants: 128
  • From 3 May 2023 to the primary completion date, 31 Dec 2027
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Presence of Neurodegenerative diseases (e.g. Parkinson's disease, Alzheimer's disease, Huntington's disease, Korsakoff's syndrome, Pick's disease, Shy-Drager syndrome)
  • History of invasive tumors or surgery in the head or neck area, except for surgeries for non-invasive skin tumors (e.g. basal cell carcinomas)
  • Permanent olfactory impairment following infections (e.g., influenza, coronavirus)
  • Conditions that, in the examiner's judgment, could interfere with the participant's study compliance (e.g., schizophrenia)

Other

  • Language barriers likely to interfere with participation or comprehension of study procedures.

Who the study is looking for

  • At least 18 years of age
  • Newly-diagnosed glioblastoma (IDH wild-type)
  • Never received prior chemotherapy
  • Never received radiotherapy to the head or neck before
  • KPS ≥ 70
  • No history of severe head or brain trauma requiring ICU admission or classified as Glasgow Coma Scale grade 3
  • No respiratory infection at the time of inclusion
  • No significant aphasia

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital Essen, Department of Neurology, Division of Clinical Neuro-Oncology
Coordinator of this site? Confirm its status
EssenGermanyRecruiting
Department of Neurosurgery
Coordinator of this site? Confirm its status
MünsterGermanyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.