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NCT06929468Recruiting

Cisplatin-induced Cochlear and Vestibular Damage in Head and Neck Cancer

Cisplatin-induced Cochlear and Vestibular Damage in Head and Neck Squamous Cell Carcinoma: A Cohort Study

Source: ClinicalTrials.gov · Last updated 20 Oct 2026

Brief summary (registry, in English)

The goal of this observational study is to learn about the occurrence of and to identify suitable strategies for screening and monitoring of inner ear damage in patients receiving cisplatin chemoradiotherapy for head and neck cancer. Researchers will compare patients who are receiving cisplatin chemoradiotherapy to patients who are only receiving radiotherapy. Patients will undergo standardized testing for hearing loss, tinnitus and vestibular dysfunction at baseline, during and after treatment. Optional genetic analyses will aim to identify genes known to predispose to cisplatin-induced ototoxicity.

Status (registry)
Recruiting
Study type
Observational
Enrollment
55 (estimated)
First submitted
7 Apr 2025
Start date
20 Jan 2026
Primary completion date
Jun 2027
Lead sponsor
Simon Jäger
NCT number
NCT06929468

What you commit to

  • Study type: Observational
  • Planned participants: 55
  • From 20 Jan 2026 to the primary completion date, Jun 2027
  • 1 site 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.

Prior treatment

  • Current cochlear implant
  • Concurrent treatment with loop diuretics (e.g. furosemide), aminoglycoside antibiotics or other known ototoxic substances in the last three months

Other illness

  • Severe hearing impairment (WHO grade 3 or 4, corresponding to an audiometric ISO value of ≥61 dB in the better ear at frequencies of 500, 1000, 2000 and 4000 Hz)
  • Acute psychosis or serious psychiatric illness
  • Addiction disorder

Other

  • Self-reported tinnitus or vestibular dysfunction in the last 3 months (only lead to exclusion of the corresponding secondary objectives, not to complete exclusion from the study)

Who the study is looking for

  • Diagnosis of head and neck squamous cell carcinoma
  • Cisplatin-based chemoradiotherapy (monotherapy or combination-therapy, adjuvant or neo-adjuvant) or only radiotherapy (control group)
  • Age 18 to 85 years
  • Signed agreement and willingness to participate in the study and adhere to the study protocol

Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Klinikum Nuremberg
Coordinator of this site? Confirm its status
NurembergGermanyRecruiting

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