Comparative Anti Helicobacter Pylori Efficacy Assessment of Unani Formulation and Quintuple Regimen
NCT ID: NCT03837210
Last Updated: 2019-02-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2/PHASE3
300 participants
INTERVENTIONAL
2017-01-05
2019-01-10
Brief Summary
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Detailed Description
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Aims and objectives
1. To establish and evaluate scientific and clinical evidence of herbal/eastern formulation and find out the clinical safety and efficacy.
2. To measure the clinical response of herbal formulation in the patients of H.Pylori.
Research Questions
1\. has the Unani formulation better effects than quadruple regimen?
Hypothesis (H1): Unani has shown better clinical, effects than quadruple regimen.
Null Hypothesis (Ho): Quadruple regimen has shown superior clinical, response than Unani formulation.
Experimental approaches
To check this hypothesis independent variable to dependent variable and perplexing variables will apply by statistical analysis. In this study H. Pylori infection, quadruple regimen are independent variables while signs and symptoms, level of improvement are dependent variables.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Test Drug
This group is treated with Herbal formulation.
Pylorin
Poly Herbal formulation
Control Drug
This group is treated with Quintuple therapy
Pylorin
Poly Herbal formulation
Interventions
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Pylorin
Poly Herbal formulation
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Individuals having no previous history of H. pylori infection treatment.
3. Individuals living in Karachi.
4. Individuals with no pathological finding on routine examination.
5. Individuals from either socioeconomic class including lower, middle and higher.
6. Both male and female individuals between 14 to 55 years of age
7. Subjects with informed written consent
8. Patients having no complications regarding other than GIT system.
Exclusion Criteria
1. Patient with simultaneous physical illness, for example renal dialysis and uncontrolled diabetes mellitus.
2. Individuals having stomach or intestinal surgical history were excluded.
3. Individuals with past record of any herbal or allopathic medication were excluded
4. Individuals with hyper sensitivity history of drug or adverse reaction to any of the study drugs .
5. Females with pregnancy were also excluded for the safety measures
6. Individuals with coma, meningitis, and encephalitis or head injury were also excluded.
7. Hospitalized individuals due to any serious diseases were excluded.
8. Individuals with known poor compliance and history of drug abuse were excluded.
15 Years
ALL
No
Sponsors
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Hamdard University
OTHER
Responsible Party
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Syed Zahoor Ul Hassan Zaidi
Syed Zahoor Ul Hassan Zaidi
Principal Investigators
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Zahoor Zaidi, M.Phil
Role: PRINCIPAL_INVESTIGATOR
Hamdard University
Other Identifiers
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zahoor11
Identifier Type: -
Identifier Source: org_study_id
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