Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01862107 · ClinicalTrials.gov registry record

Cerebrospinal Fluid Collection and Repository Storage

A clinical trial, sponsored by National Institute of Neurological Disorders and Stroke (NINDS).

Terminated
Registry status
51
Enrollment target

NCT01862107: Clinical Trial study, sponsored by National Institute of Neurological Disorders and Stroke (NINDS).

NCT01862107 is a clinical trial that was terminated before completion, run by National Institute of Neurological Disorders and Stroke (NINDS). The registered enrollment target is 51 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01862107 was terminated before completion, sponsored by National Institute of Neurological Disorders and Stroke (NINDS).

TERMINATED
Registry status
51 participants
Enrollment target

Study Summary

Background: \- Cerebrospinal fluid (CSF) is the liquid around the brain and spinal cord. Many diseases can only be diagnosed by examining the CSF. A lumbar puncture is used to collect and test CSF. Once someone is already having a lumbar puncture, a small extra amount of CSF can be collected at the same time. This fluid can be used to study brain, nerve, and related health issues. Researchers want to collect CSF and blood samples from people who are scheduled to have a lumbar puncture. Objectives: \- To collect cerebrospinal fluid and blood samples from individuals who are having a lumbar puncture. Eligibility: \- Individuals between 2 and 100 years of age who are scheduled to have a lumbar puncture for clinical or research purposes. Design: * Participants will have a lumbar puncture for clinical or research purposes. * During the procedure, an additional sample of CSF will be collected. They will also provide a blood sample, if one is not taken at the time of the procedure. * Treatment will not be provided as part of this study.

Primary Outcome

Repository of CSF and matched blood.

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2013-07-29
Est. Completion 2025-04-23

Why NCT01862107 stopped before completion

NCT01862107 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 51 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT01862107 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01862107 about?

NCT01862107 is a clinical study titled "Cerebrospinal Fluid Collection and Repository Storage". Background: \- Cerebrospinal fluid (CSF) is the liquid around the brain and spinal cord. Many diseases can only be diagnosed by examining the CSF. A lumbar puncture is used to collect and test CSF. Once someone is already having a lumbar puncture, a small extra amount of CSF can be collected at the...

What is the current status of trial NCT01862107?

This trial is currently terminated. The enrollment target is 51 participants. The study started on 2013-07-29. Estimated completion is 2025-04-23.

Who is sponsoring clinical trial NCT01862107?

This trial is sponsored by National Institute of Neurological Disorders and Stroke (NINDS), which has 567 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02701153 · 51 participants · NA

    Phase II Study of 5-Day Hypofractionated Preoperative Radiation Therapy for Soft Tissue Sarcomas: Expansion Cohort

  • NCT03663790 · 51 participants · NA

    Effects of Gait Retraining on Lower Extremity Biomechanics

  • NCT03874052 · 51 participants · Phase 1

    Ruxolitinib in Combination With Venetoclax With and Without Azacitidine in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia

  • NCT04704661 · 51 participants · Phase 1

    Testing the Combination of Two Anti-cancer Drugs, DS-8201a and AZD6738, for The Treatment of Advanced Solid Tumors Expressing the HER2 Protein or Gene, The DASH Trial

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT01862107, the US trial registry maintained by the National Library of Medicine. NCT01862107 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.