- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06851572
Prevalence of Late Xerostomia and Hyposalivation with Associated Risk Factors in Survivors of Head and Neck Cancer After Radiotherapy: a Multi-centric Cross-sectional Study
The study titled "Prevalence of Late Xerostomia and Hyposalivation with Associated Risk Factors in Survivors of Head and Neck Cancer After Radiotherapy" is a multi-centric cross-sectional study conducted in Egypt. It aims to assess the prevalence of late-onset xerostomia (dry mouth) and hyposalivation in survivors of head and neck cancer (HNC) who have undergone radiotherapy. Given the widespread use of radiotherapy as a treatment for HNC, its long-term side effects-especially on salivary gland function-are a major concern for patient quality of life.
The study includes 260 participants who have completed curative radiotherapy at least one year prior, with or without chemotherapy. Patients were selected from multiple centers, and eligibility criteria required them to be at least 18 years old. Those with recurrent or secondary malignancies were excluded. The researchers hypothesized that high doses of radiation administered to the salivary glands would lead to a high prevalence of xerostomia, and that concomitant chemotherapy might further exacerbate this condition.
To evaluate xerostomia, both subjective and objective assessments were conducted. The Summated Xerostomia Inventory (SXI), a five-item questionnaire, was used to measure self-reported symptoms of dry mouth. Objective assessments included salivary flow rate measurement, oral dryness indicators, and glandular response to stimulation. Additionally, the MD Anderson Symptom Inventory for Head and Neck Cancer (MDASI-HN) was used to assess the impact of xerostomia on daily functioning and quality of life.
The study also examined various risk factors associated with xerostomia, including tumor site, treatment type (radiotherapy alone or with chemotherapy), demographic factors (age, gender, education level), and lifestyle habits (such as smoking status). Smoking history was classified into never smokers, former smokers (quit >6 months before diagnosis), and current smokers (either quit post-diagnosis or continued smoking).
This research is significant as it is one of the first large-scale studies in Egypt to evaluate long-term salivary dysfunction in head and neck cancer survivors. By identifying prevalence rates and contributing factors, the study provides valuable insights for improving patient care and developing better management strategies for individuals suffering from post-radiotherapy xerostomia.
Study Overview
Status
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Cairo, Egypt, 11277
- Ahmed Maher Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
This study focuses on long-term survivors of head and neck cancer (HNC) who have undergone curative radiotherapy with or without chemotherapy. The population includes both male and female patients who have completed their treatment at least one year prior to participation.
Patients will be recruited from multiple medical centers, ensuring a diverse and representative sample of HNC survivors. The study aims to assess the prevalence of late-onset xerostomia and hyposalivation, along with associated risk factors such as treatment type, tumor characteristics, smoking status, and sociodemographic variables.
The study specifically targets individuals aged 18 years or older, with no recurrent or secondary primary malignancies, and who are willing to participate in subjective and objective assessments of salivary gland dysfunction.
Description
Inclusion Criteria:
- Head and Neck Cancer (HNC) Survivors
Must have completed curative radiotherapy for HNC at least 1 year prior (with or without chemotherapy).
Aged 18 years or older. Willing to provide informed consent and undergo dry mouth assessment.
Exclusion Criteria:
- Recurrent or Secondary Malignancies
Patients with recurrent HNC or a new secondary primary cancer before survey administration.
❌ Severe Comorbid Conditions
Any systemic disease or medical condition that significantly impacts salivary function (e.g., Sjögren's syndrome, uncontrolled diabetes, autoimmune diseases).
❌ Recent Radiotherapy or Ongoing Cancer Treatment
Patients who underwent radiation within the past year. Those receiving active cancer treatment during the study period.
❌ Non-Consent or Cognitive Impairment
Patients who are unwilling to participate or unable to complete questionnaires due to cognitive dysfunction.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Summated Xerostomia Inventory (SXI)
Time Frame: single point "Baseline"
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the Summated Xerostomia Inventory (SXI), which consists of five subjective statements related to dry mouth symptoms.
Each statement is scored from 1 (never) to 3 (often), with a maximum score of 15, indicating severe xerostomia.
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single point "Baseline"
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
unstimulated salivary flow rate
Time Frame: single point "Baseline"
|
Measured using unstimulated salivary flow rate collected over 5 minutes and expressed in mL/min.
Patients will be classified as having normal, reduced, or absent salivary flow.
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single point "Baseline"
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Quality of Life (QoL)
Time Frame: single point "Baseline"
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Assessed using the MD Anderson Symptom Inventory for Head and Neck Cancer (MDASI-HN), a 28-item questionnaire measuring symptom severity and daily life interference on a 0-10 scale.
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single point "Baseline"
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HAM00221
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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