A population based randomised controlled trial of Helicobacter pylori eradication: impact on dyspepsia, quality of life and health
Completed
- Conditions
- DyspepsiaDigestive System
- Registration Number
- ISRCTN44816925
- Lead Sponsor
- HS (South and West) (UK)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 1550
Inclusion Criteria
1. Aged 20 to 59 years, male and female
2. Able to give written informed consent
Exclusion Criteria
Any persons with the following conditions: pregnancy, breast feeding, severe renal impairment, adverse reaction to macrolide antibiotics, concurrent medication with wafarin, theophyllin, digoxin, terfendine, carbemazepine, ergot derivatives, bismuth compounds, acute porphyria.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Dyspepsia resolution at two years after randomisation.
- Secondary Outcome Measures
Name Time Method 1. Reduction in health service utilisation<br>2. Quality of life