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Search / Trial NCT06548776

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

Launched by M.D. ANDERSON CANCER CENTER · Aug 8, 2024

Trial Information

Current as of July 01, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is investigating a technique called Magnetic Resonance Spectroscopy (MRS) to see if it can effectively evaluate lesions (abnormal tissues) in the spinal cord. Researchers want to understand how well MRS can help in identifying changes in the spinal cord that may not be visible through other imaging methods. The trial is currently looking for participants, specifically adults over the age of 18 who do not have certain health issues like cancer, specific spinal diseases, or any history of spinal cord lesions.

To participate, individuals must be healthy or, if they are patients at high risk for a type of cancer that can affect the spinal cord, they should not show any signs of that disease in recent tests. Participants can expect to undergo some imaging tests while helping researchers learn more about how MRS can be used for spinal cord assessment. It’s important to note that this study is not for pregnant or breastfeeding individuals, those with a history of spinal surgery, or anyone with certain spinal conditions. If you think you might be eligible and are interested, you can talk to your doctor for more information.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Volunteers:
  • Adults \> 18 years
  • Healthy with no malignancy, demyelinating disease, back pain, degenerative disease, or spinal cord lesions.
  • Consent able patients.
  • Patients with high risk for LMD to receive prophylactic CNS radiation:
  • Adults \> 18 years old.
  • MR or CSF without evidence of LMD.
  • Patients with high risk for LMD to receive CSI as part of standard treatment of prophylactic LMD disease.
  • Consent able patients, willingness and ability to comply with the study procedures.
  • No spinal cord lesions.
  • Exclusion Criteria:
  • Volunteers:
  • Age \< 18 years
  • Pregnant or breastfeeding individuals.
  • History of cancer.
  • History of spinal cord lesions including malignant, demyelinating, or inflammatory.
  • History of prior spinal surgery.
  • History of implantable devices.
  • History of MR claustrophobia.
  • Degenerative disease or spinal/back pain including myelopathy and radiculopathy.
  • Scoliosis.
  • Patients with high risk for spinal LMD:
  • Age \< 18 years
  • History of spinal cord lesions including malignant, demyelinating, or inflammatory.
  • History of prior spinal surgery.
  • History of implantable devices.
  • History of MR claustrophobia.
  • Degenerative disease or spinal/back pain including myelopathy and radiculopathy.
  • Scoliosis.

About M.D. Anderson Cancer Center

The University of Texas MD Anderson Cancer Center is a leading institution dedicated to cancer care, research, education, and prevention. As one of the world’s most respected cancer centers, MD Anderson focuses on innovative treatment approaches and groundbreaking clinical trials aimed at improving patient outcomes. With a multidisciplinary team of experts and state-of-the-art facilities, the center is committed to advancing cancer research and providing comprehensive, personalized care to patients. MD Anderson's clinical trials play a pivotal role in translating scientific discoveries into effective therapies, positioning the center at the forefront of cancer treatment and research.

Locations

Houston, Texas, United States

Patients applied

0 patients applied

Trial Officials

Rami Eldaya, MD

Principal Investigator

M.D. Anderson Cancer Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported