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Comparison of Krill and Fish Oil on Clinical and Biochemical Outcomes in Depression - Trial NCT06414226

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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NCT06414226
Completed
dietary supplement
Trial Details
ClinicalTrials.gov โ€ข NCT06414226
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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

Study Focus

Depression

Krill and Fish Oil vs. Placebo

Interventional

dietary supplement

Sponsor & Location

Firat University

Adฤฑyaman, Turkey

Timeline & Enrollment

N/A

Mar 21, 2022

Oct 24, 2022

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 episode
Other depressive episodes
Recurrent depressive disorder
Recurrent depressive disorder, unspecified
Post-schizophrenic depression

Data Source

ClinicalTrials.gov

NCT06414226

Non-Device Trial