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Mastic Gum and Helicobacter Pylori eradication: an in vivo pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN01756929
Enrollment
42
Registered
2008-04-29
Start date
2006-12-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Helicobacter pylori gastritis Infections and Infestations Gastritis and duodenitis

Interventions

Patients positive to Helicobacter pylori will be randomised to receive one of the following: 1. Mastic gum 2 g per day for 14 days 2. Mastic gum 2 g per day and pantoprazole 40 mg per day for 14 day

Sponsors

The Chios Mastic Gum Producers Cooperative (Greece)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients tested positive for H. pylori 2. Adults of either sex aged between 18 and 75 years of age

Exclusion criteria

Exclusion criteria: 1. Pregnancy 2. Malignancy 3. Allergies to pantoprazole, amoxicillin, clarithromycin

Design outcomes

Primary

MeasureTime frame
Eradication of Helicobacter pylori, measured at five weeks after the end of treatment.

Secondary

MeasureTime frame
Helicobacter pylori load in patients remaining H. pylori positive, measured at five weeks after the end of treatment.

Countries

Greece

Outcome results

None listed

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