NCT06414226

Comparison of Krill and Fish Oil on Clinical and Biochemical Outcomes in Depression

Investigation of the Effect of Krill and Fish Oil Intake on Clinical and Biochemical Findings and Eating Behavior in Adult Individuals With Major Depression Disorders
Firat University·ClinicalTrials.gov·dietary supplementCompleted
View on ClinicalTrials.gov
Study focus
Disease/Condition
Depression
Drug/Device/Intervention
Krill and Fish Oil vs. Placebo
Study type
Interventional
Intervention type
dietary supplement
Sponsor & location
Primary sponsor
Firat University
Location
Adıyaman, Turkey
Timeline & enrollment
Phase
N/A
Start date
Mar 21, 2022
End date
Oct 24, 2022
Enrollment
57 participants
Primary outcome

Results of Clinical Findings,Results of Clinical Findings

Summary

The Omega-3 polyunsaturated fatty acids (n-3 PUFA), associated with fish oil, has been one of
 the most studied non-pharmacological subjects for its effect on Major Depression Disorder
 (MDD). However, studies comparing the effect of krill oil, on depression are limited, that
 has similar content and different structural forms with fish oil. This study was conducted to
 evaluate the effectiveness of the use of krill and fish oil on clinical effects, biochemical
 outcomes and eating behavior in individuals diagnosed with MDD. It was included 57 adult
 individuals diagnosed with MDD in the psychiatry clinic in this study. Randomization was
 performed after inclusion and exclusion criteria were applied in the study, and participants
 were included in one of three groups. These groups are; 1) krill oil ((n=17),
 (Eicosapentaenoic acid (EPA)=340 mg, Docosahexaenoic acid (DHA)=180 mg)), 2) fish oil
 ((n=17)), (EPA=360 mg, DHA=240 mg), 3) placebo ( (n=16), (EPA=0 mg, DHA=0 mg)). The duration
 of the intervention was 8 weeks. Anthropometric measurements, biochemical outcomes and food
 consumption records of the participants were taken at the beginning and end of the
 intervention, and Hamilton depression rating scale (HDRS), depression anxiety stress-21
 (DASS-21) and food craving questionnaire (FCQ) was applied to the participants. Statistical
 Package for Social Sciences (SPSS) and R studio software were used for statistical analysis
 of the data.

ICD-10 classifications
Depressive episodeOther depressive episodesRecurrent depressive disorderRecurrent depressive disorder, unspecifiedPost-schizophrenic depression
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06414226
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06414226 through Pure Global AI's free database. This phase not specified trial is sponsored by Firat University and is currently Completed. The study focuses on Depression. Target enrollment is 57 participants.

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