Neuroprotection With Minocycline Therapy for Acute Stroke Recovery Trial

NCT ID: NCT00930020

Last Updated: 2013-06-03

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE4
• Total Enrollment: 139 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-07-31
• Study Completion Date: 2012-11-30

Brief Summary

Background: Stroke is a leading cause of death and chronic serious disability worldwide.

Minocycline, a semisynthetic tetracycline, has consistently been shown in recent years to be neuroprotective in animal models of brain ischemia. Furthermore, a small, open label study done in humans with acute ischemic stroke published late last year showed that minocycline, when administered for 5 days, within 6 to 24 hours after stroke onset was highly effective in improving functional outcome even as early as 7 days after stroke onset. However, further well-conducted, randomized controlled translational studies using minocycline are currently lacking.

Objective: To determine if minocycline, administered within 3 to 48 hours after acute ischemic stroke onset is superior to placebo in reducing neurological deficit and improving functional outcome at 90 days post stroke.

Methods: The investigators plan to do a multi-centre randomized, double-blind, placebo controlled trial in which ischemic stroke patients will be randomized to treatment with either oral minocycline or placebo within 3 to 48 hours of symptom onset. The primary efficacy endpoint will be the modified Rankin scale (mRS) score for all randomized subjects at 90 days.

Secondary endpoints will include improvement of the NIH Stroke Scale (NIHSS) score from baseline and Barthel index at 90 days.

NeuMAST will test the following hypotheses:

Primary Hypothesis: Minocycline, compared with placebo, when administered between 3 to 48 hours after the onset of acute ischemic stroke improves recovery and functional outcome as assessed by mRS scores on day 90 post-stroke.

Secondary Hypotheses:

1. Minocycline compared to placebo, when administered between 3 to 48 hours after onset of acute ischemic stroke improves recovery and functional outcome as assessed by improvement of NIHSS score on day 90 post-stroke.

2. Minocycline compared to placebo, when administered between 3 to 48 hours after onset of acute ischemic stroke improves functional outcome as assessed by the Barthel Index (BI) score on day 90 post-stroke.

3. Minocycline, compared with placebo reduces 90 day risk of recurrent stroke, MI or death when administered between 3 to 48 hours after acute ischemic stroke onset.

A positive result will have a significant impact in the management of acute ischemic stroke and pave the way for future studies aimed at finding the optimal dose and formulation of minocycline for treating acute ischemic stroke.

Detailed Description

A) Specific Primary Objective:

1. To determine if minocycline, administered within 3 to 48 hours of acute ischemic stroke onset is superior to placebo in reducing neurological deficit and improving functional outcome on day 90 post stroke.

B) Specific Secondary Objectives:

1. To determine if minocycline administered within 3 to 48 hours of acute ischemic stroke onset is superior to placebo in reducing the 90 day risk of recurrent ischemic stroke, myocardial infarction (MI) and death.

2. To study and compare the differential efficacy of minocycline administered as stated above, on the four stroke subtypes according to TOAST criteria, i.e. lacunar stroke, large vessel atherosclerosis, cardioembolic and cryptogenic stroke

C) Primary Efficacy Endpoint:

The primary efficacy endpoint is the modified Rankin scale score at 90 days for all randomized patients.

Favorable outcome at day 90 is defined as achieving an mRS score of 0 to 1. Last observation carried forward (LOCF) will be used for subjects without assessments of the primary efficacy variable at Day 90. Deaths will be assigned a score of 6.

D) Secondary Endpoint measures:

1. NIHSS score at day 90.

2. Difference of NIHSS scores between baseline and days 7 (plus or minus 2 days) and 90 post stroke. (Favorable outcome at day 90 is defined as achieving a decrease of > 6 points on NIHSS from baseline or NIHSS < 1 at day 90.

3. mRS scores at days 7 (plus minus 2 days) and 30 post stroke.

4. Barthel index at day 90. (A score of > 85 is defined as good outcome)

5. First documentation during follow-up of ischemic stroke, myocardial infarction or death from any cause.

Recruitment of study subjects:

Acute ischemic stroke patients admitted to NNI (TTSH campus) and CGH ASU during the study period who are eligible to participate in this study based on criteria stated above will be invited to participate in this study. Approximately 1300 and 800 patients with acute ischemic stroke are admitted to NNI (TTSH campus) and CGH ASU respectively per year.

The time window for enrolment will be within 3 to 48 hours of symptom onset. For patients who are found with stroke on awakening, it will be assumed that the stroke occurred the last time that the patient was known to be normal. All eligible patients will be identified by the ward and on-call Neurology/Medical teams and referred to the study research assistants or investigators; who will then screen the patient for participation in this trial.

STUDY INTERVENTION

The assigned treatment, i.e., Minocycline 200mg or matching placebo will be administered once daily for 5 consecutive days soon after informed consent is taken and the patient is enrolled into the study.

Follow-up Assessment:

The neurologic deficits, global functional abilities and level of handicap will be scored using the NIH Stroke Scale (NIHSS) and the modified Rankin scale (mRS) at baseline and on day 7 (plus or minus 2 days).

On day 30 post-stroke, a telephone assessment with additional questions will be performed to obtain the mRS score, document any recurrent stroke, MI or death.

On day 90, in addition to a neurological evaluation, mRS and NIHSS scoring, the Barthel Index (BI) score, a measure of independence in activities of daily living, will be obtained for all subjects.

Conditions

Acute Stroke

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

matching placebo pill

matching placebo

Group Type: PLACEBO_COMPARATOR

Matched placebo

Intervention Type: DRUG

matched placebo (cornstarch) once a day for 5 days

Oral minocycline

Minocycline 200mg

Group Type: ACTIVE_COMPARATOR

Minocycline (Borymycin)

Intervention Type: DRUG

oral dose, 200 mg once a day for 5 days

Interventions

Minocycline (Borymycin)

oral dose, 200 mg once a day for 5 days

Intervention Type: DRUG

Matched placebo

matched placebo (cornstarch) once a day for 5 days

Intervention Type: DRUG

Other Intervention Names

Borymycin; Placebo - cornstarch

Eligibility Criteria

Inclusion Criteria

• Singapore citizens or permanent residents
• Age range between 21 to 80 years
• NIHSS equal or more than 5 but less than 22 at time of admission
• Clinical diagnosis of acute ischemic stroke according to WHO criteria
• Onset of stroke between 3 to 48 hours prior to start of treatment
• Must have a working telephone line

Exclusion Criteria

• Long term residents of Institutions and Nursing homes
• Patients with significant baseline cognitive dysfunction
• Patients with hemorrhagic stroke
• Pre-stroke MRS more than 1
• Evidence of other disease of the CNS (i.e., brain tumor, CNS infections)
• Known allergic response to tetracycline
• Acute or Chronic renal failure
• Hepatitis or liver disease
• Pre-existing infectious disease requiring antibiotics
• Receipts of IV rTPA
• Participation in another clinical trial in the preceding 3 months
• Unable or unwilling to provide inform consent
• Unwilling to return for frequent clinic visits
• Geographic or social factors making the study participation impractical

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Neuroscience Institute

OTHER

Sponsor Role: collaborator

Changi General Hospital

OTHER

Sponsor Role: collaborator

Singhealth Foundation

OTHER_GOV

Sponsor Role: lead

Responsible Party

Dr. Rajinder Singh

Dr

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Rajinder Singh, Doctor

Role: PRINCIPAL_INVESTIGATOR

National Neuroscience Institute - Tan Tock Seng campus and Changi hospital

Locations

National Neuroscience Institute - Tan Tock Seng hospital

Singapore, , Singapore

Countries

Singapore

References

Lampl Y, Boaz M, Gilad R, Lorberboym M, Dabby R, Rapoport A, Anca-Hershkowitz M, Sadeh M. Minocycline treatment in acute stroke: an open-label, evaluator-blinded study. Neurology. 2007 Oct 2;69(14):1404-10. doi: 10.1212/01.wnl.0000277487.04281.db.

Reference Type: BACKGROUND

PMID: 17909152 (View on PubMed)

Other Identifiers

SHF/CTG016/2008

Identifier Type: -

Identifier Source: org_study_id