Clinical trial · Observational
Post-radiotherapy Rhinosinusitis in Children
Evaluation of Chronic Rhinosinusitis in Children Managed for Cervicofacial Mesenchymal Malignancy
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): COVID
Summary
Brief summary (as posted)
Chronic rhinosinusitis (CRS) is a frequent complication of facial cancer treatment, mainly related to radiotherapy. However, while radiological involvement is frequent, clinical expression seems less important. Few studies have investigated the incidence of this condition in the pediatric population while its evolution seems to be very chronic even if a partial improvement may occur with time. Our objective is therefore to study the impact of CSR in children treated for cancer of the cervicofacial region, to evaluate its incidence and medium-term evolution in order to determine whether it is necessary to set up a specific follow-up in these patients. The clinical impact of CSR is assessed by a specific SNOT 22 questionnaire in children treated for a head-neck mesenchymal malignancy in comparison with a control population consisting of children treated for a mesenchymal malignancy of non-head-neck location.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Chronic Sinusitis | — | UNRESOLVED | — |
| Pediatric Cancer | Childhood Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| SNOT 22 questionnaire | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- Exposed patients
- interventionNames
- Other: SNOT 22 questionnaire
- label
- Non exposed patients
Primary outcomes (1)
- measure
- Impact of CRS in pediatric patients by Sino-Nasal Outcome Test-22 (SNOT 22)
- timeFrame
- >1 year to <4 years after the end of oncologic treatment
Secondary outcomes (5)
- measure
- Incidence of CRS in pediatric patients after head neck mesenchymal cancer management
- timeFrame
- 1 year after the end of the oncologic treatment
- measure
- Correlation between SNOT 22 and clinical assessment by PADORES score
Eligibility
Eligibility (as posted)
- Sex
- All
- Maximum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Study population: all patients under 18 years of age managed for a head neck mesenchymal cancer between January 1, 2018 and December 31, 2024 * Control population: all patient under 1 years of age managed for non -head neck mesenchymal cancer between January 1, 2018 and December 31, 2024 Exclusion Criteria: * Patients with hematological tumors; * Patients with mucociliary pathologies or proven allergic rhinitis before the diagnosis of cancer * Patients who have required surgical treatment that has removed more than half of the sinus cavities * Tumor recurrence at the time of inclusion * Sinus surgery between the last radiological check-up and inclusion * Administrative reasons: inability to receive informed information.
References
Publications (0)
Data not yet available