Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:06 AM
Ignite Modification Date:
2025-12-25 @ 2:06 AM
NCT ID:
NCT04785560
Eligibility Criteria:
FOR iNPH-PATIENTS:
INCLUSION CRITERIA:
* Must meet the clinical criteria for iNPH according to the International Guide lines of 2005
* Must undergo shunt implantation at the Dpt of Neurosurgery Linköping University Hospital.
EXCLUSION CRITERIA:
* Individuals not able to participate/cooperate in study tasks with regard to cognitive symptoms
* Individuals with claustrophobia that makes awake MRI examination impossible.
* Individuals with implants that make MRI examination impossible (for instance pacemaker, refers only to the MRI examinations included in the study).
* Patients with severe co-existing chronical neurological diseases (refers only to the proteomic examinations included in the study).
FOR CONTROL GROUP VOLUNTEERS:
INCLUSION CRITERIA:
* Must undergo surgery under spinal anesthesia at the Dpt of Orthopaedics, Urology or Gynaecology at the University Hospital Linkoping.
* Must consider themselves neurologically healthy and have not undergone neurological disease.
EXCLUSION CRITERIA:
* Individuals with claustrophobia that makes awake MRI examination impossible.
* Individuals with implants that make MRI examination impossible
* Individuals with malignant disease or oncological treatment for such disease.
* Individuals with neurological disorders detected after study MRI.
Healthy Volunteers:
True
Sex:
ALL
Study:
NCT04785560
Study Brief:
Protocol Section:
NCT04785560