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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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16 October 2023 |
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Main ID: |
NCT03547544 |
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Date of registration:
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23/05/2018 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Rapid Urease Test for Diagnosis Helicobacter Pylori Infection
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Scientific title:
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Effectiveness of Rapid Urease Test (Helicotec) for The Diagnosis of Helicobacter Pylori Infection in Dyspepsia Patients in Endoscopy Centre |
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Date of first enrolment:
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May 28, 2018 |
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Target sample size:
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97 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/ct2/show/NCT03547544 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Indonesia
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Contacts
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Name:
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Ari F Syam, Dr, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Gastroenterology Division, Internal Medicine Department RSCM/UI |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Adult (18-55 years old),
- Diagnosed with dyspepsia,
- Indicated for endoscopy,
- Agreed to participate in the study and signed the informed consent.
Exclusion Criteria:
- Pregnancy and breastfeeding woman,
- Patients with alarm symptom,
- History taking of antibiotics (amoxicillin, clarithromycin, levofloxacin), H2 receptor
antagonist, proton pump inhibitor, misoprostol, sucralfat, bismuth, NSAIDs, steroid,
rheumatoid drug within the last 2 weeks.
Age minimum:
18 Years
Age maximum:
55 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Helicobacter Pylori Infection
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Primary Outcome(s)
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Effectivity of Helicotec
[Time Frame: 1 day]
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Secondary ID(s)
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18-04-0394
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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