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Spots Global Cancer Trial Database for Neurocognition After Radiotherapy in CNS- and Skull-base Tumors

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Trial Identification

Brief Title: Neurocognition After Radiotherapy in CNS- and Skull-base Tumors

Official Title: Neurocognition After Radiotherapy in Adult Brain and Base of Skull Tumors

Study ID: NCT05727605

Study Description

Brief Summary: The goal of this multicenter prospective longitudinal study is to study the long-term impact of multimodal treatment (chemotherapy, radiotherapy and surgery) in adult brain and base of skull tumors on neurocognitive functioning. All included patients will complete a self-report inventory (subjective cognitive functioning, QoL, confounders), a cognitive test battery, an advanced MR at multiple timepoints. Moreover, toxicity will be scored according to the CTCAEv5.0 in these patients over time.

Detailed Description: This study will combine MR imaging techniques together with elaborate neuropsychological assessments and RT dosimetry in 120 patients who will be examined baseline (before RT) and followed longitudinally after RT. The first objective is to build an NTCP model for neurocognitive decline after RT (for each cognitive domain separately), linking dose-volume parameters to structures within the brain susceptible to neurological damage and neurocognitive decline after radiotherapy. These NTCP models can be used to make predictions on neurocognitive decline in future primary brain tumour patients receiving cranial RT. The second objective is to evaluate dose-dependent neurocognitive decline. In particular, the investigators will assess: * Prevalence and severity of neurocognitive decline after RT for all cognitive domains * Brain structures or functional brain connections important in neurocognitive functioning (based on dedicated MRI). * Dose-dependencies of specific neurocognitive skills after RT in adult brain tumour patients * Correlations between RT dosimetry and early brain changes (MRI)

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University Hospitals Ghent, Gent, , Belgium

UZ Leuven, Leuven, , Belgium

Gasthuis Zusters Antwerpen, Wilrijk, , Belgium

Contact Details

Name: Maarten Lambrecht, MD PhD

Affiliation: UZ Leuven

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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