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

NCT00836355 · ClinicalTrials.gov registry record · NA

Enoxaparin and/or Minocycline in Acute Stroke

A NA study, sponsored by NYU Langone Health.

Terminated
Registry status
NA
Development phase
6
Enrollment target

NCT00836355: Clinical Trial NA study, sponsored by NYU Langone Health.

NCT00836355 is a NA study that was terminated before completion, run by NYU Langone Health. The registered enrollment target is 6 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00836355, a NA study, was terminated before completion, sponsored by NYU Langone Health.

TERMINATED
Registry status
NA
Development phase
6 participants
Enrollment target

Study Summary

The purpose of this study is to investigate whether enoxaparin, minocycline, or both medications in combination may help in recovery from acute stroke. Enoxaparin (brand name Lovenox®) is a medication approved for use in humans to prevent and to treat blood clots in deep veins in certain specific medical situations. Minocycline (brand name Minocin®) is a tetracycline antibiotic approved to treat a number of bacterial infections in humans. The investigators are studying these medications in acute human stroke because they have each been separately shown to reduce the amount of injured brain tissue in rats made to have acute ischemic stroke experimentally. In a human trial comparing minocycline with placebo (a sugar pill) acute ischemic stroke patients who took minocycline had better recovery after 1 week, 1 month and 3 months than patients who took placebo.

Interventions

  • DRUG Enoxaparin
  • DRUG Minocycline

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2009-04
Est. Completion 2010-01
Phase NA
NYU Langone Health

1,164 total trials

Why NCT00836355 stopped before completion

NCT00836355 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 2 interventions - of which Enoxaparin is the first listed.

NCT00836355 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00836355 about?

NCT00836355 is a clinical study titled "Enoxaparin and/or Minocycline in Acute Stroke". The purpose of this study is to investigate whether enoxaparin, minocycline, or both medications in combination may help in recovery from acute stroke. Enoxaparin (brand name Lovenox®) is a medication approved for use in humans to prevent and to treat blood clots in deep veins in certain specific m...

What is the current status of trial NCT00836355?

This trial is currently terminated. It is a NA study. The enrollment target is 6 participants. The study started on 2009-04. Estimated completion is 2010-01.

What interventions are being tested in trial NCT00836355?

The interventions under investigation include: Enoxaparin (DRUG), Minocycline (DRUG).

Who is sponsoring clinical trial NCT00836355?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00836355's enrollment target sits among peer trials

6 1983rd of 2000 higher than 13 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

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

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00836355, the US trial registry maintained by the National Library of Medicine. NCT00836355 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.