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Clinical Trials in the Netherlands / NCT06046625
Active, not recruiting Observational

Needs and Preferences of Patients With Head-neck Cutaneous SCC

NCT06046625 · tracked via the Priya Life Science Netherlands tracker
Phase
Observational
Started
2021-11-01
Last updated
2025-04-04

Condition(s) studied

Cutaneous Squamous Cell CarcinomaCutaneous Squamous Cell Carcinoma of the Head and NeckSquamous Cell CarcinomaSquamous Cell Carcinoma of Head and NeckSquamous Cell Carcinoma of the Head and NeckSkin CancerPatient SatisfactionHigh-Risk CancerPreference, PatientDecision MakingInterview

Investigational drug(s) / intervention(s)

Regular care with additional administration of a semi-structured interview

Regular care with additional administration of a semi-structured interview: Patients receiving regular care. In addition, a semi-structured interview is conducted. The semi-structured interviews take place once after completion of the care pathway (after all appointments for check-ups associated with the treatment). The interview contains questions about the experience of patients with the care, the needs in this care, the experiences with the information received, the support/guidance, the turnaround time, the treatment received and areas for improvement.

Study summary

The care of patients with high-risk cutaneous squamous cell carcinomas in the head-neck area is complex and requires a multidisciplinary approach. A key component in this care is the need and experience of patients. However, studies on the experiences and needs of patients with high-risk cutaneous squamous cell carcinomas in the head-neck region are lacking.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients diagnosed with a cSCC, located in the head-neck region * who visited the multidisciplinary head-neck team of the Maastricht University Medical Center+ * who already received treatment for their cSCC * who gave informed consent for participation Exclusion Criteria: \- patients who are cognitively impaired for participation in an interview

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Maastricht University Medical Center+ Maastricht Netherlands

More Maastricht University Medical Center trials in the Netherlands

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06046625 on ClinicalTrials.gov ↗ ← All trials in the Netherlands