MR imaging biomarkers associated with patient-reported xerostomia post-RT

Recruiting

• Conditions: Speekselklier schade naar aanleiding van hoofdhals radiotherapie; dry mouth syndrome; Xerostomia

• Registration Number: NL-OMON54312
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 9 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 54

Inclusion Criteria

• The patients are above 18 years old and have received (chemo)radiotherapy for
primary H&N cancer with curative intent.
• Patients can be enrolled after completion of their radiotherapy treatment
months from 6 months up to 3 years.
• The patients have no previous history of surgery in H&N region.
• The patients have provided written informed consent before inclusion in the
study.

Exclusion Criteria

• The patients have adverse-indication for an MRI scan, such as claustrophobia,
pregnancy, pacemaker or implantable defibrillator, metal implants.
• Patients with psychological or somatic disorders, limiting the possibilities
for adequate follow-up.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified