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Use of Minocicline in Patients With Stroke

H

Hospital Universitario Hernando Moncaleano Perdomo

Status and phase

Unknown
Phase 1

Conditions

Brain Ischemia
Stroke
Paralysis

Treatments

Drug: Placebo
Drug: Minocicline

Study type

Interventional

Funder types

Other

Identifiers

NCT01556802
38212050

Details and patient eligibility

About

The investigators will evaluate the National Institute of Health Stroke Scale/Score (NIHSS)in patients with stroke, and then give Minocycline 100mg po every 12 hours or placebo for five days, then perform periodic evaluations to determine the status and degree of neurological sequelae developed.

Enrollment

134 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • NIHSS scale greater than 5
  • Onset of symptoms less than 24 hours
  • normal Cranial Tomography(CT)
  • CT evidence of cerebral ischemia
  • Acceptance of study entry

Exclusion criteria

  • Hemorrhagic cerebrovascular disease
  • Other neurological diseases
  • Concomitant structural damage
  • History of neurosurgery
  • Known allergy to tetracyclines
  • Concomitant infectious diseases requiring antibiotic treatment.
  • History of Stroke
  • Women pregnant or breast-feeding

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

134 participants in 2 patient groups, including a placebo group

Minocicline
Experimental group
Description:
minocicline 100mg oral twice a day for 5 days
Treatment:
Drug: Minocicline
Placebo
Placebo Comparator group
Description:
Pills filled with vegetal fiber with similar presentation of the drug. Given one pill oral twice a day for five days
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Central trial contact

Nataly Bedoya, md

Data sourced from clinicaltrials.gov

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