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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01863277
Other study ID # 0130-12
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received May 22, 2013
Last updated May 24, 2013
Start date July 2013

Study information

Verified date April 2013
Source Wolfson Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug AdministrationIsrael: Ministry of Health
Study type Interventional

Clinical Trial Summary

The purpose of the study is to evaluate the effect of Melatonin (in a dosage of 14mg daily) for a better clinical outcome in the period three days post stroke.


Description:

Stroke is the third most common cause of stroke. The cascade of event is separated into hyperacute,,acute,sub-acute and chronic. In the acute, sub acute state there are mechanisms of inflammation apoptotic death and effect of free radicals. Melatonin was proved to effect these mechanisms and to have a favourable effect in different diseases. The aim of the study is to prove That the use of Melatonin in a higher dosage may have a anti-destructive effect in stoke.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 140
Est. completion date
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- within 72hours of ischemic stroke

- age 18-80

- both gender

- ability to sign consent form

Exclusion Criteria:

- intra-cerebral bleeding

- tumour of brain

- multiple sclerosis

- s/p craniotomy

- known allergy to melatonin

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Melatonin

placebo


Locations

Country Name City State
Israel E. Wolfson Medical Center Holon

Sponsors (1)

Lead Sponsor Collaborator
Wolfson Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement of at least one point on the MRS score 3 months No
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