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

Not Applicable
Conditions
Helicobacter pylori.
Registration Number
IRCT201101122709N16
Lead Sponsor
Vive-chancellor for Research, Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
105
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

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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).
Secondary Outcome Measures
NameTimeMethod
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