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Assesment of hearing in patients of head and neck cancer undergoing concurrent chemoradiotherapy: a hospital based study.

Assesment of hearing outcome in patients of head and neck cancer undergoing concurrent chemo radiotherapy: a hospital based study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/06/112511
Enrollment
100
Registered
2026-06-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C148- Malignant neoplasm of overlappingsites of lip, oral cavity and pharynx

Interventions

Intervention1: Nil: Nil

Sponsors

Dr Himanshu Negi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients of head and neck cancer with primary site of malignancy at nasal cavity, nasopharynx, oral cavity, oropharynx, larynx, hypopharynx and salivary glands undergoing concurrent chemoradiotherapy

Exclusion criteria

Exclusion criteria: Patient with prior history of radiation exposure. Patient with a known history of pre existing sensorineural hearing loss or middle ear pathology. Patient with history of receiving ototoxic drugs. Patient who are known case of Type 2 Diabetes Mellitus or Chronic Kidney Disease.

Design outcomes

Primary

MeasureTime frame
To assess the incidence and severity of hearing loss in patients of head and neck cancer undergoing concurrent chemoradiotherapy using pre and post treatment Pure Tone AudiometryTimepoint: To assess the incidence and severity of hearing loss in patients of head and neck cancer undergoing concurrent chemoradiotherapy using pre and post treatment Pure Tone Audiometry(PTA), PTA will be assessed before start of chemoradiotherapy and then finally after 6 months of baseline PTA

Secondary

MeasureTime frame
To document the change in hearing thresholds across different frequencies (250 Hz - 8000Hz) post concurrent chemoradiotherapyTimepoint: From before start of chemoradiotherapy to after completion of chemoradiotherapy

Countries

India

Contacts

Public ContactDr. Shahzad Ahmad

GMC HALDWANI

drshahzadjnmch@yahoo.com9634623901

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026