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The effect of natural turpentine Kurdica on Helicobacter pylori

Phase 2
Conditions
H. pylori infection of the stomach.
Other and unspecified infectious diseases
Registration Number
IRCT2016042527599N1
Lead Sponsor
Vice chancellor for Research Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
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

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pulmonary function changes. Timepoint: 2 days before and 30 days after the intervention. Method of measurement: According to the DOB.
Secondary Outcome Measures
NameTimeMethod
Headache - abdominal pain - diarrhea - nausea. Timepoint: During the intervention. Method of measurement: Qualitative.
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