About this trial
More than half of all pediatric cancer in Korea are solid cancer. For the treatment of solid cancer, multidisciplinary methods such as surgery, chemotherapy, and radiation therapy are applied, and with the development of the treatment method, the treatment performance has improved dramatically, and the 5-year survival rate of more than 80% is currently recorded. Due to the improvement in survival rate, interest in side effects caused by cancer treatment itself is gradually increasing, and efforts to reduce them are increasing. Accordingly, it aims to contribute to improving the quality of life of pediatric solid cancer survivors. by developing a Korean-type early diagnosis and follow-up protocol of ototoxic hearing loss, which commonly occurs in pediatric solid cancer who have undergone chemotherapy.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
Those who have difficulty understanding the clinical trial due to mental retardation or unable to read the consent form, such as illiteracy or foreigners ③ Those who have difficulty in hearing test due to neurological factors, etc. ④ Other cases judged to be inappropriate for this study by the judgment of the person in charge of the clinical trial
Trial population
Patients who are diagnosed as solid cancer and receive platinum chemotherapy
Trial design
Cohort
Prospective
Treatments tested in this trial
Chemotherapy involving cisplatin or carboplatin
Other interventionChemotherapy
Treatment groups
Trial outcomes
Primary outcomes
Proportion of patients with ototoxic hearing loss
Proportion of patients with ototoxic hearing loss in total patients
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: