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Effect of high protein regime in nurocritical patients

Comparison of the Effectiveness of High-protein Nutritional regimes with Normal regimes on Neuronal Bio-markers and Clinical Outcome of Neurocritical Patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120703010178N14
Enrollment
30
Registered
2018-04-11
Start date
2018-04-04
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Diseases of the nervous system injury. Diffuse traumatic brain injury

Interventions

Intervention 1: Intervention group: Prescribing protein (1.5-2 mg/kg/day) for 5 days. Intervention 2: Control group: Prescribing a regular diet in the intensive care unit for 5 days.

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients older than 16 years old who have one of the following factors and stay in ICU for 5 days. Subarachnoid Hemorrhage Subdural Hematoma Traumatic brain injury Aneurysm Intracranial hemorrhage Others

Exclusion criteria

Exclusion criteria: Patient's death during the first three days of study Patient dis-admit with personal satisfaction within the first three days Disapprove of the patient to enter the research Contraindication of receiving high protein die Hepatic encephalopathy An allergy to the drug Consumer of Warfarin Pregnancy Metabolic disorders (gout, phenylketonuria) Chronic renal failure Proteinuria is higher than 3 grams per day

Design outcomes

Primary

MeasureTime frame
Neuron Specific Enolase. Timepoint: At the beginning of the intervention (before the intervention) and 3 and 5 days after the beginning of the intervention. Method of measurement: Enolase CanAg kit.;Serum Transtreatin Level. Timepoint: At the beginning of the intervention (before the intervention) and 3 and 5 days after the beginning of the intervention. Method of measurement: Prealbumin Minineph *25T.;Nitrogen Balance. Timepoint: At the beginning of the intervention (before the intervention) and 5 days after the beginning of the intervention. Method of measurement: Based on urea concentration.

Secondary

MeasureTime frame
Extended Glasgow Outcome Scale. Timepoint: The end of the first, second and third months after the begining intervention. Method of measurement: Score of Extended Glasgow Outcome Scale.;Mortality. Timepoint: The end of the first, second and third months after the begining intervention. Method of measurement: Will be checked by phone.;Effect of medication on neuron specific Enolase. Timepoint: At the beginning of the intervention (before the intervention) and 3 and 5 days after the beginning of the intervention. Method of measurement: Blood sample.;Effect of medication on serum prealbumin level. Timepoint: At the beginning of the intervention (before the intervention) and 3 and 5 days after the beginning of the intervention. Method of measurement: blood sample.;Effect of medication on nitrogen balance. Timepoint: At the beginning of the intervention (before the intervention) and 5 days after the beginning of the intervention. Method of measurement: Urine sample.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Sistanizad

Shahid Beheshti University of Medical Sciences

sistanizadm@sbmu.ac.ir+98 21 8820 0087

Outcome results

None listed

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