Skip to content

The Comparison of The Effect of Eicosapentaenoic Acid and Docosahexaenoic Acid on Helicobacter pylori Infection Eradication and Some Serum Inflammatory Factors

The Comparison of The Effect of Eicosapentaenoic Acid and Docosahexaenoic Acid on Helicobacter pylori Infection Eradication and Some Serum Inflammatory Factors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201101122709N16
Enrollment
105
Registered
2011-02-13
Start date
2011-01-30
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

Helicobacter pylori.

Interventions

Intervention 1: control group : MCT supplement, 2 grams per day (twice a day, each time 1 gram), at morning and evening, and during 12 weeks. Intervention 2: intervention 1 group : moreEPA supplement,
Placebo
Treatment - Drugs
control group : MCT supplement, 2 grams per day (twice a day, each time 1 gram), at morning and evening, and during 12 weeks
intervention 1 group : moreEPA supplement, 2 gram per day (twice a day, each time 1 gram) at morning and evening, and during 12 weeks
intervention 2 group:moreDHA supplement, 2 grams per day (twice a day, each time 1 gram), at morning and evening, and during 12 weeks

Sponsors

Vive-chancellor for Research, Tehran University of Medical Sciences
Lead Sponsor
Gastrointestinal & Liver Disease Research Center (Firoozgar GILDRC)
Collaborator

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: - positive stool antigen test result - no history of pharmaceutical treatment for infection eradication - no gastric surgery - no history of peptic ulcer - no any disease that cause inflammation & increase of serum inflammatori markers level such as diabetes, CVD, respiratoryinflammations such as asthma,... - no consumption of any drug other than prescribed drugs during the study - no consumption of antibiotic or bismut during 2 months before the trial - no consumption of antioxidant supplements such as Se, Zn, beta-caroten,... at least 3 months before the trial - no consumption of omega-3 supplements at least 3 months before the trial - no smoking - BMI less than 30 - age between 20-60 years old -leaning to cooperation Exclusion criteria: - no leaning to continuing the cooperation - any change in type or dose of prescribed drugs - any change in daily diet or physical activity - consumption of any antioxidant supplement - consumption of less than 70% of supplements given to patients at the start of the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Helicobacter pylori infection eradication. Timepoint: before & after intervention (after 12 weeks intervention). Method of measurement: stool antigen test.;Serum level of Il-6. Timepoint: before & after intervention (after 12 weeks intervention). Method of measurement: ELISA kitt.;Serum level of Il-8. Timepoint: before & after intervention (after 12 weeks intervention). Method of measurement: ELISA kitt.;Serum level of hs-CRP. Timepoint: before & after intervention (after 12 weeks intervention). Method of measurement: ELISA kitt.;Serum level of TAC. Timepoint: before & after intervention (after 12 weeks intervention). Method of measurement: colorimetry (FRAP).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Farzad Shidfar

Faculty of Public Health of Tehran University of Medical Sciences

farzadshidfar@yahoo.com+98 21 8877 9118

Outcome results

None listed

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