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Effects of nanocurcumin in treatment of patients with Helicobacter pylori

Investigating the effects of nano curcumin in eradicating and improving the symptoms of patients with Helicobacter pylori infection

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230131057297N1
Enrollment
80
Registered
2023-05-09
Start date
2023-06-01
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Helicobacter pylori infection. Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters

Interventions

Intervention 1: Intervention group: Nanocurcumin capsule 40 mg every 8 hours (Exir Nano Sina Company) + Levofloxacin 500 mg daily + Omeprazole 20 mg every 12 hours + Amoxicillin 1 gr every 12 hours fo

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Having informed consent to enter the study People aged 18 to 70 years with digestive symptoms such as dyspepsia, nausea, vomiting and epigastric burning Any person who does not have any of the exclusion criteria

Exclusion criteria

Exclusion criteria: History of anti-Helicobacter pylori treatment Taking antibiotics Acute gastrointestinal bleeding Proton pump inhibitor use in the last month Pregnancy or breastfeeding Allergy to turmeric and ginger family Known cancers including stomach People with HIV Recent surgeries Alcohol consumption and the presence of systemic diseases such as cardiovascular diseases and diabetes

Design outcomes

Primary

MeasureTime frame
Hong Kong dyspepsia index. Timepoint: before the intervention, immediately after the intervention and one month after the end of the intervention. Method of measurement: Hong Kong dyspepsia index.;Helicobacter pylori eradication rate. Timepoint: One month after treatment. Method of measurement: Stool antigen test.

Secondary

MeasureTime frame
Frequency of clinical symptoms (dyspepsia, nausea, vomiting and epigastric burning) in the intervention and placebo groups. Timepoint: The beginning and end of the study. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadali mahdiabadi

Birjand University of Medical Sciences

mahdiabadi_ma@bums.ac.ir+98 56 3162 2035

Outcome results

None listed

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