Dyspepsia Clinical Trial
Official title:
Prospective, Randomized Controlled Trial Comparing Amoxicillin and Metronidazole Based Bismuth-containing Quadruple Therapy With Amoxicillin and Clarithromycin Based Quadruple Therapy for First-line Helicobacter Pylori Eradication
No trial has examined the the efficacy of amoxicillin and metronidazole based quadruple therapy for Helicobacter pylori treatment. The study aims to compare the effectiveness and safety of 14-day amoxicillin-/metronidazole-based quadruple regiment and classical quadruple regiment for Helicobacter pylori eradication.
Helicobacter pylori is the most successful human pathogen infecting an estimated 50% of the
global population. It is a common and potentially curable cause of dyspepsia and peptic
ulcer disease. Eradication in patients with peptic ulcer or even functional or
non-investigated dyspepsia is a cost effective approach.
Most Consensus Conferences and Clinical Guidelines recommend the prescription of a triple
therapy including a proton pump inhibitor (PPI) and clarithromycin with either amoxicillin
or metronidazole, as first-line treatment. However, the effectiveness of these
triple-therapy regimens seems to have diminished over time, largely as a result of emerging
resistance of the organism to clarithromycin. Due to the low efficacy achieved with these
treatments, they have been deemed as unethical comparators in clinical trials. As
antimicrobial resistance becomes more prevalent worldwide, treatment failure rates are
likely to continue increasing, suggesting that new regimens for H pylori eradication must be
sought.
Bismuth-containing quadruple therapies have been used widely in H. pylori therapy with many
permutations of doses and durations and with variable results. Classical bismuth-based
quadruple therapy containing a PPI, bismuth, tetracycline and metronidazole has been
recommended as the first-line treatment by the Maastricht IV Consensus Conference report and
H. pylori Study Group of Chinese Society of Gastroenterology. But this regiment has high
rate of side effects because of tetracycline. Standard triple therapy-based,
bismuth-containing quadruple Therapy is also an alternative. Though addition bismuth and
prolonging treatment duration can overcome H. pylori resistance to clarithromycin, its use
as a first-line treatment is limited in areas of high clarithromycin resistance.
Amoxicillin has low resistance rate as well as low percentage of side effects. The
combination of amoxicillin and metronidazole in bismuth-containing quadruple therapy may be
a better choice, which can avoid clarithromycin resistance and reduce side effects.
Therefore, we will do a randomized trial to compare the eradication rate of 14-day
amoxicillin and metronidazole based bismuth-containing quadruple therapy with amoxicillin
and clarithromycin based quadruple therapy for Helicobacter pylori infection.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06094062 -
Smartphone App-assisted PPI
|
N/A | |
Completed |
NCT03941288 -
Efficacy and Safety of Cannabidiol for Gastroparesis and Functional Dyspepsia
|
Phase 2 | |
Completed |
NCT04429802 -
The Effect of Prucalopride (Resolor®) on Gastric Motor Function and Gastric Sensitivity
|
N/A | |
Not yet recruiting |
NCT06369753 -
Visible Abdominal Distension
|
N/A | |
Withdrawn |
NCT02863822 -
Study to Evaluate Dietary Modification in Patients With Functional Dyspepsia.
|
N/A | |
Recruiting |
NCT00978159 -
Esomeprazole or Famotidine in the Management of Aspirin Related Non-Ulcer Dyspepsia
|
Phase 4 | |
Completed |
NCT00723502 -
Efficacy and Safety Study of Finafloxacin Used in Helicobacter Pylori Infected Patients
|
Phase 2 | |
Terminated |
NCT00220844 -
Tricyclic Antidepressants (TCAs) on Gastric Emptying
|
N/A | |
Completed |
NCT00217347 -
Evaluation of Efficiency of Esophageal Capsule Endoscopy in the Screening of Patients With Gastroesophageal Reflux Disease or Dyspepsia as Compared to Upper Endoscopy
|
N/A | |
Completed |
NCT00148603 -
Montelukast in the Treatment of Duodenal Eosinophilia
|
N/A | |
Completed |
NCT00164996 -
Ultrathin Versus Conventional Esophagogastroduodenoscopy in Unsedated Patient With or Without Local Pharyngeal Anaesthesia
|
Phase 3 | |
Completed |
NCT00110968 -
Long-term Safety and Efficacy of Itopride Hydrochloride (HCl) in Patients Suffering From Functional Dyspepsia
|
Phase 3 | |
Completed |
NCT00232102 -
Extension Study to Assess the Long-Term Safety of Tegaserod in Women With Symptoms of Dyspepsia
|
Phase 3 | |
Completed |
NCT00232037 -
Extension Study to Assess the Long-Term Safety of Tegaserod in Women With Symptoms of Dyspepsia
|
Phase 3 | |
Recruiting |
NCT05718960 -
Traditional Dietary Advice Versus Reassurance-alone in Postprandial Functional Dyspepsia
|
N/A | |
Terminated |
NCT04247100 -
A Study of Randomized Sham-control Auricular TENS Unit Stimulation in Pediatric Functional Gastrointestinal Disorders
|
N/A | |
Completed |
NCT05750641 -
The Efficacy of Removal of Animal Milk From the Diet in Functional Dyspepsia: A Cross-sectional Study
|
||
Completed |
NCT04697641 -
Helicobacter Pylori Eradication in Functional Dyspepsia
|
N/A | |
Completed |
NCT03252743 -
ICBT for Pain-predominant FGIDs in Children and Adolescents: an Implementation Study.
|
N/A | |
Recruiting |
NCT04918329 -
Functional Digestive Disorders Observatory
|