NCT05927610

Genetic Testing of Cerebrospinal Fluid to Diagnose and Monitor Glioblastoma

Evaluating the Role of Cerebrospinal Fluid (CSF) Cell-free DNA (cfDNA) as a Prognostic Biomarker in Glioblastoma
Memorial Sloan Kettering Cancer Center·ClinicalTrials.gov·diagnostic testRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Glioblastoma
Drug/Device/Intervention
Lumber Puncture
Study type
Observational
Intervention type
diagnostic test
Sponsor & location
Primary sponsor
Memorial Sloan Kettering Cancer Center
Location
New York, United States of America
Timeline & enrollment
Phase
N/A
Start date
Jun 19, 2023
End date
Jun 19, 2028
Enrollment
180 participants
Primary outcome

Overall Survival

Summary

The goal of this study is to determine the utility of cerebrospinal fluid (CSF) cell-free DNA
 (cfDNA) as a prognostic biomarker in glioblastoma (GBM).

ICD-10 classifications
Malignant neoplasm of brainMalignant neoplasm: Brain, unspecifiedMesotheliomaMalignant neoplasm: Brain stemMalignant neoplasm: Overlapping lesion of brain
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05927610
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05927610 through Pure Global AI's free database. This phase not specified trial is sponsored by Memorial Sloan Kettering Cancer Center and is currently Recruiting. The study focuses on Glioblastoma. Target enrollment is 180 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.