Skip to main content
Clinical Trials/NCT01674582
NCT01674582
Completed
Not Applicable

Treatment Effects Inclusive Cognitive Impact and Possibilities to Individually Adjusted Treatment in Patients With Intracranial Tumors With Clinical, Neuropsychological and Imaging Parameters.

Lund University Hospital1 site in 1 country150 target enrollmentOctober 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intracranial Tumor
Sponsor
Lund University Hospital
Enrollment
150
Locations
1
Primary Endpoint
Early prediction of treatment response based on MRI parameters.
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The main purposes with this trial is to investigate the potential of MRI with diffusion and blood volume, flow in brain to diagnose and to measure treatment effects in patients with intracranial tumors, especially gliomas and metastases in a prospective trial, to evaluate the possibilities to individually adjusted treatment in this category of patients depending on treatment outcomes measured by MRI, to perform clinical follow up in connection with MRI to evaluate a correlation and to perform testing of cognitive ability before, during, and after treatment and to investigate if given treatment causes any decrease in the patients habitual state.

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
December 31, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age 18 years or older
  • Suspected primary brain tumor, verified glioblastoma or non surgically treated metastases from solid tumor
  • Increasing MRI changes in patients with previous verified glioblastoma
  • Be able to speak Swedish without difficulties (because of the neuropsychological investigations)
  • Written informed concent

Exclusion Criteria

  • Unability to perform MRI

Outcomes

Primary Outcomes

Early prediction of treatment response based on MRI parameters.

Time Frame: Three weeks compared to baseline.

Secondary Outcomes

  • Neuropsychological function.(Month 3, 12, and 18 compared to baseline)

Study Sites (1)

Loading locations...

Similar Trials