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Effect of new drugs sodium ozagrel and edaravone in treatment of stroke

Phase 4
Conditions
Health Condition 1: null- Acute ischaemic Stroke
Registration Number
CTRI/2012/05/002644
Lead Sponsor
JIPMER
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
168
Inclusion Criteria

1.Patients with atherothrombotic stroke presenting after 4.5 hrs and within 24 hrs of onset with objective neurological deficits

2.Above 18 years of age and gives informed consent (patient/relative)

Exclusion Criteria

1.Cardio embolic stroke

2.Intracerebral hemorrhage (including subarachnoid hemorrhage, subdural hemorrhage, extradural hemorrhage)

3.Patients who have received thrombolytic therapy tPA

4.Patients who are receiving heparin for any reason

5.Renal impairment (creatinine >2 mg/dl)

6.Hepatic dysfunction (clinical or abnormal LFT)

7.Bleeding diathesis

8.Recent major surgery within one month or minor surgery within two weeks of stroke

9.NIHSS <4 or more than 22.

10.Congestive cardiac failure or other conditions where saline infusion of 1000 ml/day will be risky

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary outcome measure â??3 month functional outcome assessed using Modified Rankin Scale (MRS) <br/ ><br> <br/ ><br>Secondary outcome measures- NIH score or SSS and Barthel index at day 14 and 1 month, Intracranial haemorrhage, Renal failure, hepatic dysfunction or any unexplained organ function abnormality, seventh day and thirtieth day. All adverse events and SAEs will be reported as per GCP guidelines. <br/ ><br>Timepoint: at discharge/death and at 3 months
Secondary Outcome Measures
NameTimeMethod
Secondary outcome measures- NIH score or SSS and Barthel index at day 14 and 1 month, Intracranial haemorrhage, Renal failure, hepatic dysfunction or any unexplained organ function abnormality, seventh day and thirtieth day. All adverse events and SAEs will be reported as per GCP guidelines.Timepoint: day 0, 14 and 1 month
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