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Evaluation of the effect of pyloricin soft gel on Helicobacter pylori infection

Evaluation of the effect of soft gel containing essential oil of Satureja hortensis(pyloricin) on eradicating and clinical symptoms of Helicobacter pylori infection

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130211012438N27
Enrollment
60
Registered
2018-09-19
Start date
2018-08-23
Completion date
Unknown
Last updated
2018-10-11

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 elsewhere

Interventions

Intervention 1: Intervention group:Routin treatment(Omeprazole20(Produced in Abidi Pharmaceutical Company) +Amoxicillin1+ Clarithromycin500(Produced in Toliddaru Pharmaceutical Company) BID)+ Herbal

Sponsors

Barij Research Center of Medicinal Herbs
Lead Sponsor
Vice chancellor for research of Kashan University of Medical Sciences
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Confirmation of Helicobacter Pylori infection by gastroenterologist with the help of a sample of pathology taken in the endoscopy or a positive result of anti-Helicobacter pylori antibodies in the serum sample of patients Patients with functional dyspepsia or gastroduodenal ulcer have indications of eradication of Helicobacter pylori infection

Exclusion criteria

Exclusion criteria: A person with advanced chronic disease Any allergy to the drugs used in the study Pregnancy or breastfeeding Substance abuse or alcohol use Having a history of treatment to eradicate Helicobacter pylori infection Taking antibiotics or bismuth 4 weeks before entering the study Constipation

Design outcomes

Primary

MeasureTime frame
Clinical signs. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.;Eradication rate of helicobacter pylori. Timepoint: after 1 months from the end of treatment. Method of measurement: stool antigen for helicobacter pylori.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactM.Taghizadeh

Kashan University of Medical Sciences

taghizadeh_m@kaums.ac.ir+98 36 1555 0021

Outcome results

None listed

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