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The effect of omega-3 in the prevention of delirium in intensive care unit

The effect of omega-3 clinical trial in the prevention of delirium in hospitalized patients in intensive care unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201509055363N5
Enrollment
164
Registered
2015-11-20
Start date
2015-09-23
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

delirium. Other delirium

Interventions

Intervention 1: Patients who are in the drug group will be gavage with 2 grams of omega-3 daily. Intervention 2: In the control group placebo (syrup, methyl cellulose) will be gavage.
Treatment - Drugs
Patients who are in the drug group will be gavage with 2 grams of omega-3 daily.
In the control group placebo (syrup, methyl cellulose) will be gavage.

Sponsors

Vice- Chancellor for Research of Zanjan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: APACHEE score under 25; GCS=7-9; age over 18 years; Patients under mechanical ventilation; No history of dementia-Alzheimer and Parkinson; No use of anti-psychotic drugs; No history of allergy to omega-3 or fish; Patients who are not suffering from brain damage; Patients who were admitted due to surgical complications in the intensive care unit Exclusion criteria: Separated from the ventilator in less than 72 hours; Death in less than 48 hours; Discharge from the ICU in under 72 hours

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Number of days without delirium during the first 7 days of hospitalization. Timepoint: Twice daily. Method of measurement: CAM-ICU: Confusion assestment method for the ICU.

Secondary

MeasureTime frame
Mortality during hospitalization in ICU. Timepoint: End of the study. Method of measurement: Records.;The number of days that patients are not connected to ventilator in the ICU stay. Timepoint: End of the study. Method of measurement: Records.;The number of ICU days stay. Timepoint: End of the study. Method of measurement: Records.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNavid Shafigh

Zanjan University of Medical Sciences

Navid_shafigh2005@yahoo.com+98 24 3347 2865

Outcome results

None listed

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