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neuroprotective effects of L-Carnitine and Fat emulsion in the CVA Ischemic patients

Evaluation neuroprotective effects of L-Carnitine and Fat emulsion in the CVA patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201510043014N11
Enrollment
60
Registered
2017-03-11
Start date
2016-09-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cerebrovascular accident ischemic. Cerebrovascular accident NOS

Interventions

Intervention 1: Intervention group 1: Infusion 500 cc intralipid during 12 hours per day for 7 days. Intervention 2: Intervention group 3: Prescription 10 cc L-Carnitine per day for 7 days and infusio
Treatment - Drugs
Treatment - Other
Intervention group 1: Infusion 500 cc intralipid during 12 hours per day for 7 days
Intervention group 3: Prescription 10 cc L-Carnitine per day for 7 days and infusion 500 cc intralipid during 12 hours per day for 7 days
Intervention group 2: Prescription 10 cc L-Carnitine per day for 7 days
Control group: Without intervention by L-Carnitine and intralipid

Sponsors

Vice chancellor for research, Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
21 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: CVA ischemic MCA inpatient, admitted during first 24 hours after the onset of symptoms, 21-75 years old Exclusion criteria: less than 21years old and more than 75 years old, hepatic failure( rise hepatic enzymes >5nl, cirrhosis), treatment by valproate, treatment by hemodialysis, sepsis, ARDS, triglyceride > 400, acute pancreatitis plus hyperlipidemia, plt < 70000, signs and symptoms appearance more than 72 hours before admission, CNS infections, seizure, migraine.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Neuron specific enolase: NSE. Timepoint: base, 24hr after admission, 48hr after admission, 7th days after admission. Method of measurement: 5 cc serum plasma.;S100B. Timepoint: base, 24hr after admission, 48hr after admission, 7th days after admission. Method of measurement: 5 cc serum plasma.;Lactate dehydrogenase. Timepoint: base, 24hr after admission, 48hr after admission, 7th days after admission. Method of measurement: 5 cc serum plasma.;Pirovate dehydrogenase. Timepoint: base, 24hr after admission, 48hr after admission, 7th days after admission. Method of measurement: 5 cc serum plasma.

Secondary

MeasureTime frame
Evaluation neurologic outcomes : Neurologic examination of GCS, cranial nerves, motor nerves, sensory nerves. Timepoint: At admission time and when Discharge from hospital. Method of measurement: Physical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Shahram Ala

Mazandaran University Of Medical Sciences

sala@mazums.ac.ir+98 11 3354 3084

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026