RECRUITING

Establishing Daily Applicable Parameters for Using Magnetic Resonance Spectroscopy of Spinal Cord

Talk to us

Conditions

Spinal Cord

Quick Navigation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

To learn if MRS can effectively assess spinal cord lesions.

Official Title

Establishing Daily Applicable Parameters for Using Magnetic Resonance Spectroscopy of Spinal Cord

Quick Facts

Study Start:2024-09-04
Study Completion:2027-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06548776

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adults \> 18 years
  2. * Healthy with no malignancy, demyelinating disease, back pain, degenerative disease, or spinal cord lesions.
  3. * Consent able patients.
  4. * Adults \> 18 years old.
  5. * MR or CSF without evidence of LMD.
  6. * Patients with high risk for LMD to receive CSI as part of standard treatment of prophylactic LMD disease.
  7. * Consent able patients, willingness and ability to comply with the study procedures.
  8. * No spinal cord lesions.
  1. * Age \< 18 years
  2. * Pregnant or breastfeeding individuals.
  3. * History of cancer.
  4. * History of spinal cord lesions including malignant, demyelinating, or inflammatory.
  5. * History of prior spinal surgery.
  6. * History of implantable devices.
  7. * History of MR claustrophobia.
  8. * Degenerative disease or spinal/back pain including myelopathy and radiculopathy.
  9. * Scoliosis.
  10. * Age \< 18 years
  11. * History of spinal cord lesions including malignant, demyelinating, or inflammatory.
  12. * History of prior spinal surgery.
  13. * History of implantable devices.
  14. * History of MR claustrophobia.
  15. * Degenerative disease or spinal/back pain including myelopathy and radiculopathy.
  16. * Scoliosis.

Contacts and Locations

Study Contact

Rami Eldaya, MD
CONTACT
(713) 745-2945
reldaya@mdanderson.org

Principal Investigator

Rami Eldaya, MD
PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center

Study Locations (Sites)

MD Anderson Cancer Center
Houston, Texas, 77090
United States

Collaborators and Investigators

Sponsor: M.D. Anderson Cancer Center

  • Rami Eldaya, MD, PRINCIPAL_INVESTIGATOR, M.D. Anderson Cancer Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-09-04
Study Completion Date2027-07-31

Study Record Updates

Study Start Date2024-09-04
Study Completion Date2027-07-31

Terms related to this study

Additional Relevant MeSH Terms

  • Spinal Cord