Bacterial Infection Due to Helicobacter Pylori (H. Pylori) Clinical Trial
Official title:
A Randomized Controlled Trial of Triple Therapy Versus Sequential Therapy Versus Concomitant Therapy as First Line Treatment for Helicobacter Pylori Infection
Triple therapy (TT) comprising proton pump inhibitor (PPI), amoxicillin 1g and
clarithromycin 500mg twice daily has long been considered one of the standard treatment for
H. pylori infection as initial studies demonstrated success rates of > 90% on per protocol
analysis (PP) and > 80% on intention to treat (ITT) analysis. However increasing bacterial
resistance, especially to clarithromycin, has been reported and there are concerns that the
efficacy of TT has decreased. Sequential therapy (ST) is an alternative first line therapy
that consists of 5 days of treatment with a PPI and amoxicillin followed by 5-day treatment
with the PPI and clarithromycin and metronidazole. The rationale for this approach is that
amoxicillin may weaken the bacterial cell wall in the initial phase of treatment, and
prevent the development of drug efflux channels that inhibit clarithromycin from binding to
ribosomes and thus help to improve the efficacy of clarithromycin in the second phase of
treatment. A recent meta-analysis based on mainly European studies showed that the success
rate of ST compared to TT was 92.8 - 96% vs. 76.2 - 78.8%. Concomitant therapy (CT) is
another alternative first line treatment that consists of 10 days of PPI, amoxicillin,
clarithromycin and metronidazole. The rationale for using CT as a first line treatment
option is to address the possibility of clarithromycin resistance which is increasingly
encountered in clinical practice. Currently there are no randomized controlled studies that
compared TT with ST in Singapore, although both regimens are being used in routine clinical
practice. The hypothesis is that ST is superior to TT as first line treatment for H. pylori
infection.
The study aim to compare 10-day TT versus 10-day ST versus 10-day CT as first line treatment
for H. pylori infection in Singapore.
Background Helicobacter pylori is a common infection in Singapore with an overall
seroprevalence rate of 31%. The prevalence rate increases with age and exceeds 70% among
those more than 65 years of age (1). H pylori is a major pathogen and is associated with
development of peptic ulcer disease and gastric malignancies and successful H. pylori
eradication has been shown to be important for both primary and secondary prevention of
these diseases (2). Triple therapy (TT) comprising proton pump inhibitor (PPI), amoxicillin
1g and clarithromycin 500mg twice daily has long been considered one of the standard
treatment for H. pylori infection (2, 3) as initial studies demonstrated success rates of >
90% on per protocol analysis (PP) and > 80% on intention to treat (ITT) analysis . However
increasing bacterial resistance, especially to clarithromycin, has been reported and there
are concerns that the efficacy of TT has decreased. Sequential therapy (ST) is an
alternative first line therapy that consists of 5 days of treatment with a PPI and
amoxicillin followed by 5-day treatment with the PPI and clarithromycin and metronidazole.
The rationale for this approach is that amoxicillin may weaken the bacterial cell wall in
the initial phase of treatment, and prevent the development of drug efflux channels that
inhibit clarithromycin from binding to ribosomes and thus help to improve the efficacy of
clarithromycin in the second phase of treatment. A recent meta-analysis based on mainly
European studies showed that the success rate of ST compared to TT was 92.8 - 96% vs. 76.2 -
78.8% (4). Concomitant therapy (CT) is another alternative first line treatment that
consists of 10 days of PPI, amoxicillin, clarithromycin and metronidazole. The rationale for
using CT as a first line treatment option is to address the possibility of clarithromycin
resistance which is increasingly encountered in clinical practice (5). Currently there are
no randomized controlled studies that compared TT with ST in Singapore, although both
regimens are being used in routine clinical practice. The hypothesis is that ST is superior
to TT as first line treatment for H. pylori infection.
Aim 10-day triple therapy (TT) [twice daily proton pump inhibitors (PPI), amoxicillin 1 g
and clarithromycin 500mg] versus 10-day sequential therapy (ST) [5 day PPI and amoxicillin
1g twice daily followed by 5 days PPI, clarithromycin 500mg and metronidazole 400mg twice
daily] versus 10-day concomitant therapy (CT) [twice daily PPI, amoxicillin 1g,
clarithromycin 500mg and metronidazole 400mg] as first line treatment for H. pylori
infection.
Patients and Methods
Study Design:
Prospective randomized controlled study.
Treatment H. pylori infected patients will be randomized to be treated using either 10 day
TT (PPI, amoxicillin 1g, clarithromycin 500mg twice daily) or 10-day ST (PPI and amoxicillin
1 g twice daily x 5 days followed by PPI, clarithromycin 500mg, metronidazole 400mg twice
daily x 5days) or 10-day CT (PPI, amoxicillin 1g, clarithromycin 500mg, metronidazole 400mg
twice daily). The success of treatment will be defined as either a negative carbon urea
breath test (CUBT) or negative histology performed more than 4 weeks after completion of
treatment. CUBT or histology will be performed based on the clinical indication as
determined by the attending physician. All patients should be off PPI for at least 2 weeks,
or histamine 2 receptor antagonists for at least 1 week, prior to assessment of the success
of treatment, as per standard practice. The compliance to treatment in terms of percentage
of drugs taken will be assessed during clinic review.
Antibiotic susceptibility testing For patients with H. pylori infection diagnosed during
endoscopy from a positive rapid urease test kit, the material from the test kit will be used
sent for antibiotic susceptibility testing whenever it is technically feasible. This may be
of value in guiding the choice of antibiotics for second line salvage treatment should first
line treatment fails.
Statistical analysis:
A treatment success rate of 80% is regarded as the minimum acceptable threshold for empiric
first line therapy. Data from several countries have suggested that the success rate of
triple therapy may be lower than 80%, whereas that for concomitant therapy may exceed 90%.
Thus for the study to have 80% power with significance level of 5%, the minimum number of
patients to be recruited into each arm will be 138 if the highest success rate is 91% and
lowest success rate is 79%. Randomization will be performed in blocks of 15. Categorical
data will be analysed using Chi-square or Fisher exact test, while continuous data will be
analysed using student's t test. A p value of < 0.05 will be taken as statistically
significant.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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