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The effect of natural turpentine Kurdica on Helicobacter pylori

Investigating the effect of oral administration of Pistacia Atlantica Kurdica gum on the eradication of H.pylori in patients with dyspepsia symptoms: a randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016042527599N1
Enrollment
100
Registered
2016-05-25
Start date
2015-06-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

H. pylori infection of the stomach. Other and unspecified infectious diseases

Interventions

Intervention group 2: intervention group 1 drugs plus two capsules containing 500mg of powdered Pistacia Atlantica kurdica bd for 14 days.
Intervention 1: Control group: Two placebo capsules, 500 mg (bd) for 14 days. Intervention 2: Intervention group 1: 500 mg of Amoxicillin bd, Clarithromycin 500 mg bd and Omeprazole 20 mg bd, obtained
Placebo
Treatment - Drugs
Control group: Two placebo capsules, 500 mg (bd) for 14 days
Intervention group 1: 500 mg of Amoxicillin bd, Clarithromycin 500 mg bd and Omeprazole 20 mg bd, obtained from Pharmaceutical Sobhan for 14 days
Intervention group 3: two capsules containing two 500mg of powdered Pistacia Atlantica kurdica obtained from Department of Pharmacology, Shiraz University of Medical Sciences bd for 14 days

Sponsors

Vice chancellor for Research Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria Gastrointestinal clinic patients 20 to 40 years old; UBT positive symptoms of indigestion; avoiding the use of antibiotics Exclusion criteria Pregnancy and lactation; the development of pharmaceutical agents stopped the study; travel or unwillingness to continue treatment; lack of medication; taking the wrong medication

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pulmonary function changes. Timepoint: 2 days before and 30 days after the intervention. Method of measurement: According to the DOB.

Secondary

MeasureTime frame
Headache - abdominal pain - diarrhea - nausea. Timepoint: During the intervention. Method of measurement: Qualitative.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamidollah Afrasiabian,MD

Research Center for Traditional Medicine and History of Medicine, Shiraz University of Medical Scien

afrasiabian@sums.ac.ir+98 21 2273 0456

Outcome results

None listed

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