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Status unknownNCT01388127MinocyclineUpdated Jul 6, 2011

Minocycline Treatment in Acute Hemorrhagic Stroke

An observational study in Poor Performance Status, sponsored by Wolfson Medical Center. Status unknown at 1 site in Israel. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2011-07-06.

Sponsored by Wolfson Medical Center · Observational

The sponsor has not verified this record recently (last verified Jun 2011), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
150
Ages
18 Years to 90 Years
Sex
All
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Study summary

The investigators will perform a double blind controlled study to investigate the efficacy of oral administration of 200 mg minocycline, on the neurological and functional outcome after acute hemorrhagic stroke and the effect on blood brain barrier permeability.

Read the detailed description

Minocycline, a semisynthetic second generation derivative of tetracycline, was shown to have a clear beneficial neuroprotective effect in animal models of multiple sclerosis, Parkinson's disease, Huntington's disease and amyotrophic lateral sclerosis. Animal models provide promising evidence of minocycline's ability to improve outcomes in an animal stroke model.

In light of these findings, we will perform a double blind controlled study to investigate the efficacy of oral administration of 200 mg minocycline, on the neurological and functional outcome after acute hemorrhagic stroke and the effect on blood brain barrier permeability.

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Conditions studied

  • Poor Performance Status

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In context

Hemorrhagic Stroke

214 studies on the registry are indexed under Hemorrhagic Stroke; 84 are open to participants now.

This study's planned enrollment of 150 is below the median of 300 across 64 observational studies indexed under Hemorrhagic Stroke.

Browse Hemorrhagic Stroke studies →

Lead sponsor

Wolfson Medical Center is the lead sponsor of 113 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

150 patients after acute hemorrhagic stroke. Half treated with Minocycline.

Inclusion criteria

  • Patients with acute hemorrhagic stroke

    1. age > 18
    2. NIHSS score > 5
    3. onset of stroke 6 to 24 hours prior to beginning of treatment. Patients, who arrived within 0 to 6 hours post stroke, were treated with other medications according to the best accepted medical treatment guidelines.

Exclusion criteria

Exclusion Criteria:

  1. Evidence of other disease of the central nervous system, including brain tumor, demyelinating disease, inflammatory disease of the central nervous system, craniotomy in the past, severe brain injuries and benign intracranial hypertension
  2. pre-existing neurological disability
  3. known allergic response to tetracyclines
  4. acute or chronic renal failure
  5. pre-existing infectious disease requiring antibiotic therapy
  6. swallowing difficulties
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
150 participants (estimated)
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Study locations

1 site
  • Edith Wolfson Medical Center
    Holon, 58100, Israel
    • Yair Lampl, MD · Contact · y_lampl@hotmail.com · 972-3-5028512
    • Yair Lampl, MD · Principal investigator
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 6, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01388127
Lead sponsor
Wolfson Medical Center
First posted
Jul 6, 2011
Start date
Jul 2011
Primary completion
Jul 2012 (estimated)
Completion
Jul 2012 (estimated)
Last update
Jul 6, 2011

Study contacts

Yair Lampl, MD
principal investigator · Edith Wolfson Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2011. You cannot join it, but the record below documents what was studied.

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