Stroke Patients Presenting Within 24 Hrs of Onset of Symptoms
Conditions
Keywords
Stroke, HES, Coagulation, Kinetics, Hemorehology
Brief summary
The use of HES has been found clinically to improve patients with stroke if administered within a window period by means of hemodilution to improve rehology. We propose to see the effects of long term administraion of HES in the amounts required for treating stroke patients and study the effects on the kinetics of HES, its effects on coagulation and hemorheology.
Detailed description
Patients with stroke benefit with hemodilution when administered HES in a window period and continued for a period of 10 days. Hemodilution improves the hemorheology and thus possibly preserves the cerebral tissues in the penumbra regions of affected vessels. We propose to see the effects of prolonged administration of HES from different makes and study the kinetics, hemorehology and coagulation parameters by TEG as there is no literature on kinetics and coagulation follwing prolonged use in stroke patients and also study their neurological outcomes. Patients presenting to the Emergency department or outpatient department within 24 hrs of manifestation of symptoms will be recruited to the study after taking informed consent in a language the patients/ family understand by the study personnel identified and authorized to do the same. The patients will then be randomly allocated to receive HES of either make for 10 day with 10 patients in each group. The randomization is by random number generation by computer. The product is blinded to the patient and observer by black cover with only the label A OR B of each group. Blood Samples will be drawn at time of randomization, after 3, 5 and 10 days for rehological, coagulation effects and kinetics of HES, stored as per requirements and analyzed. Routine biochemical tests as prescribed by the physician will be undertaken as required. Satistical analysis of data will be done by SPSS.
Interventions
DRUGHES administration
DRUGHydroxy Ethyl Starch administration to stroke patients
Sponsors
Nizam's Institute of Medical Sciences University, India
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
Age 18 - 70 yrs Clinical diagnosis of ischemic stroke No marked spontaneous improvement of symptoms before randomization Written informed consent from nearest relative. \-
Exclusion criteria
Pregnancy Allergy to HES Severe impairment of consciousness Previous stroke with persistent ipsilateral deficits. Seizure at stroke onset. Intracranial neoplasm or AV malformation. Cardiac insufficiency or pulmonary edema Myocardial infarction during the previous 3 months or unstable angina. Severe dehydration Coagulation disorders. Uncontrolled Hypertension. Laboratory findings reflecting severe anemia, renal insufficiency, thrombocytopenia or hepatic insufficiency. Participation in another clinical trial within the previous 2 months or concurrent treatment with any other experimental drug. SECONDARY
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patients discharged from hospital | — |
Secondary
| Measure | Time frame |
|---|---|
| Coagulation, rehology and kinetics measurements. | — |
Outcome results
None listed