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Exploratory Biomarker Study of Cerebrospinal Fluid in Healthy Volunteers

NCT01126567 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 8

Last updated 2010-05-19

No results posted yet for this study

Summary

The objective of this study is to determine the effects of cerebrospinal fluid sampling rate on biomarker levels of young, healthy volunteers.

Conditions

  • Healthy

Interventions

OTHER

Sampling Rate

Both cohorts will have a lumbar catheter placed and CSF samples will be obtained. The only difference between the two arms will be the sampling rate of CSF. One arm will have a high sampling rate and the other will have a low sampling rate.

Sponsors & Collaborators

Principal Investigators

  • Robert Lenz, M.D., Ph.D. · Abbott

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-12-31
Primary Completion
2010-01-31
Completion
2010-02-28

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01126567 on ClinicalTrials.gov