Memantine for the Reduction of Cognitive Impairment After Radiation Therapy in Pediatric Patients With Central Nervous System Tumors
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- STATUS
- Recruiting
-
- participants needed
- 20
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- sponsor
- Mayo Clinic
Summary
This early phase I trial studies the feasibility of giving
Description
PRIMARY OBJECTIVE:
I. To evaluate the feasibility of twice daily
SECONDARY OBJECTIVE:
I. To evaluate the feasibility of twice daily (BID)
EXPLORATORY OBJECTIVES:
I. To evaluate the change in neurocognitive function (NCF) as found by formal neurocognitive testing between baseline and 12 months post-RT.
II. To compare the change in NCF between baseline and the end of RT, 3,and 6 months after RT
using both
III. To evaluate changes in quantitative volumetric
IV. To correlate cognitive changes detected by CogState composite score and formal
V. Disease-free (of
- OUTLINE
Patients receive
After completion of study, patients are followed up periodically.
Details
Condition | Malignant Central Nervous System Neoplasm, Primary Central Nervous System Neoplasm |
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Age | 4years - 18years |
Treatment |
Cogstate Assessment Battery,
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Clinical Study Identifier | NCT04217694 |
Sponsor | Mayo Clinic |
Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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