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Effect of alfa-lipoic acid on important outcomes in patients admitted to intensive care units

Effect of alfa lipoic acid on biochemical and nutritional status and important outcomes in patients admitted to intensive care unit.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201302083236N4
Enrollment
80
Registered
2013-06-06
Start date
2013-02-19
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

patients admitted in Intensive Care Unit.

Interventions

Intervention 1: alfa-lipoic acid 900mg/day for 10 days. Intervention 2: placebo for 10 days.
Treatment - Drugs
Placebo
alfa-lipoic acid 900mg/day for 10 days
placebo for 10 days

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: age=18; expected length of stay more than 7 days; using enteral feeding method during admitted to ICU. Exclusion criteria: having the history of autoimmune disease, severe renal or liver failure, AIDS, hepatitis; having severe malnutrition at the admission time; having TPN at the admission time in ICU; extreme intolerance to enteral feeding.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Length of stay in ICU. Timepoint: at the end. Method of measurement: days.;Mortality. Timepoint: at the end. Method of measurement: number and percent.;Ventilator free days. Timepoint: during ICU stay. Method of measurement: daily assessment.

Secondary

MeasureTime frame
Insulin resistance. Timepoint: first and last days of intervention. Method of measurement: HOMA calculation equation.;Sequential organ failure assessment score. Timepoint: first and last days of intervention. Method of measurement: sequential organ failure assessment score questioniar.;Malondialdehyde. Timepoint: first and last days of intervention. Method of measurement: spectrophotometery.;Total antioxidant capacity. Timepoint: first and last days of intervention. Method of measurement: ELIZA.;C reactive protein. Timepoint: first and last days of intervention. Method of measurement: nephelometry.;Interleukin-6. Timepoint: first and last days of intervention. Method of measurement: ELIZA.;Albumin. Timepoint: first and last days of intervention. Method of measurement: ELIZA.;PreAlbumin. Timepoint: first and last days of intervention. Method of measurement: Turbidimetry.;Total lymphocyte count. Timepoint: first and last days of intervention. Method of measurement: microscopic count.;Mid arm circumference. Timepoint: first and last days of intervention. Method of measurement: centimeter.;Total protein. Timepoint: first and last days of intervention. Method of measurement: based on labratory measurement.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactnajmeh hejazi

shiraz university of medical sciences- nutrition department

n20hejazi@yahoo.com+98 71 1725 1001

Outcome results

None listed

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