Skip to content

Eradication of Helicobacter

Study of probiotic and simvastatin additive effect on Helicobacter eradication rate

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180130038566N1
Enrollment
160
Registered
2018-05-13
Start date
2017-03-21
Completion date
Unknown
Last updated
2018-06-18

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

Conditions

Helicobacter pylori. Helicobacter pylori [H. pylori] as the cause of diseases classified elsewhere

Interventions

Intervention 1: Simvastatin 10 mg - Sobhan Iran Co. - Required quantity or amount 560. Intervention 2: Simvastatin 20 mg - Sobhan Iran Co. - Required amount or amount of 560. Intervention 3: Daily Pro

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Is over 18 years old. Is satisfied. In terms of Helicobacter pylori, it has not been treated until now.

Exclusion criteria

Exclusion criteria: Dissatisfaction. Have a history of recent antibiotic intake. Contra has indications of receiving probiotic or simvastatin, or when it comes to drug use during drug use. alcohol consumption. smoking.

Design outcomes

Primary

MeasureTime frame
Eradication rate of Helicobacter pylori. Timepoint: Patients are treated for two weeks, after which treatment is discontinued and four weeks after completion of the treatment, a fecal antigen test for eradication of Helicobacter pylori infection is examined. Method of measurement: Measurement of Helicobacter pylori in Ahvaz Imam Khomeini Hospital Laboratory.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbazar Parsi

Ahvaz University of Medical Sciences

dr_abazar_parsi@yahoo.com+98 61 3311

Outcome results

None listed

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