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Arachidonic acid supplementation to improve cognitive impairment of schizophrenia

Exploring the impact and underlying mechanisms of arachidonic acid supplementation on cognitive impairment in schizophrenia: a double-blinded, placebo-controlled, randomized study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN31248612
Enrollment
80
Registered
2024-07-05
Start date
2020-11-08
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Schizophrenia Mental and Behavioural Disorders

Interventions

This was designed for a double-blinded, placebo-controlled, randomized clinical trial (RCT) of oral arachidonic acid (AA) supplementation to identify whether the adjunctive intervention can improve co

Sponsors

National Natural Science Foundation of China
Lead Sponsor
Shanghai Jiao Tong University
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients of SZ were diagnosed according to the International Classification of Diseases 10th edition (ICD-10) 2. The patient's family members or legal guardians fully understood the content of this study and signed informed consent

Exclusion criteria

Exclusion criteria: 1. Patients should not have a history of other mental disorders, neurological disorders, serious physical diseases, traumatic brain injury, substance abuse, or dependence 2. Healthy controls should not have any current or previous psychiatric history or family history, as assessed by the Mini-International Neuropsychiatric Interview (M.I.N.I.)

Design outcomes

Primary

MeasureTime frame
Cognitive function was measured using the Cambridge Neuropsychological Test Automated Battery® (CANTAB®) system at baseline, week 3, and 6

Secondary

MeasureTime frame
1. RBC's lipids and fatty acids were measured using gas chromatography-mass spectrometry at baseline and week 6 2. Mitochondria lipids measured using ultrahigh-performance liquid chromatography quadrupole orbitrap mass spectrometry at baseline and endpoint 3. RNA sequencing of white blood cells was conducted at baseline and endpoint 4. Niacin skin flushing response test using 6 concentrations (triple gradient dilution from 60 mM) of niacin dropped onto the skin at baseline, week 3, and 6

Countries

China

Contacts

Public ContactXiaowen;Yan Hu;Gao

;

xiaowen@sjtu.edu.cn;Gao_Yan@sjtu.edu.cn+ 86 21 62833148;+ 86 21 62833148

Outcome results

None listed

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