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Helicobacter Pylori Infection clinical trials

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NCT ID: NCT04850209 Completed - Clinical trials for Helicobacter Pylori Infection

The Impact of WeChat Group Patient Education on the Eradication Rate of Helicobacter Pylori

Start date: July 23, 2021
Phase: N/A
Study type: Interventional

In this study, effects of oral and written education, WeChat education plus oral and written education on Helicobacter pylori eradication will be compared in a randomized way.

NCT ID: NCT04708405 Completed - Clinical trials for Inflammatory Bowel Diseases

The Relationship Between Helicobacter Pylori Infection and Inflammatory Bowel Diseases: A Real-life Observation

Start date: September 10, 2019
Phase:
Study type: Observational

Numerous epidemiological studies have investigated the association between Helicobacter pylori (H. pylori) infection and inflammatory bowel disease (IBD) with various conflicting results. The main objective of this study is to further explore the possible association between H. pylori infection and IBD and its impact on disease course. The investigators sought to conduct a prospective observational study and enroll a total of 182 IBD patients who were screened for H. pylori infection. All the participants will be clinically evaluated at the initial visit and bimonthly for 3 months. Several factors will be explored such are diet, physical activity, life style and considering specific environmental exposures that impact the development of disease or its relapse.

NCT ID: NCT04697641 Completed - Clinical trials for Helicobacter Pylori Infection

Helicobacter Pylori Eradication in Functional Dyspepsia

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

This study is designed to study benefit of eradicating Helicobacter Pylori in patients with functional dyspepsia as compared to symptomatic treatment only. Helicobacter pylori positive patients with Functional Dyspepsia will be divided into two study groups, one will receive Helicobacter pylori eradication therapy and other will receive symptomatic treatment. Symptom relief based on Likert scale will be compared in both groups.

NCT ID: NCT04697186 Completed - Gastric Cancer Clinical Trials

Helicobacter Pylori Eradication With Berberine Plus Amoxicillin Triple Therapy Versus Bismuth-containing Quadruple Therapy

Start date: January 7, 2021
Phase: Phase 4
Study type: Interventional

This study aims at evaluating efficacy and safety of berberine hydrochloride, amoxicillin and rabeprazole triple therapy versus bismuth-containing quadruple therapy(amoxicillin, clarithromycin, rabeprazole and bismuth) in the first eradication treatment of H. pylori. It is hypothesized that berberinehydrochloride, amoxicillin and rabeprazole triple therapy is non-inferior to bismuth-containing quadruple therapy. Patients diagnosed with H. pylori infection will be randomly divided into one of the above treatments. At week 6 follow-up visits, a urea breath test,rapid urease test or helicobacter pylori stool antigen test will be performed to confirm eradication.

NCT ID: NCT04678492 Completed - Gastric Cancer Clinical Trials

Helicobacter Rescue Therapy With High-dose Esomeprazole and Amoxicillin Dual Therapy Versus Bismuth-containing Quadruple Therapy

Start date: December 20, 2020
Phase: Phase 4
Study type: Interventional

This study aims at evaluating efficacy and safety of high-dose esomeprazole and amoxicillin dual therapy(esomeprazole and amoxicillin) versus bismuth-containing quadruple Therapy(bismuth,esomeprazole,tetracycline and furazolidone) in H. pylori rescue therapy. It is hypothesized that high-dose esomeprazole and amoxicillin dual therapy is non-inferior to bismuth-containing quadruple Therapy. Patients with confirmed failure of H. pylori eradication will be randomized to one of the treatments described above. At week 6 follow-up visits, a urea breath test,rapid urease test or helicobacter pylori stool antigen test will be performed to confirm eradication.

NCT ID: NCT04660123 Completed - Gastric Cancer Clinical Trials

A Real World Study of Bismuth Colloidal Pectin Granules Quadruple Therapy for H. Pylori Eradication

Start date: December 20, 2020
Phase: Phase 4
Study type: Interventional

To observe the eradication rate of H. pylori infection, symptom improvement and the incidence of adverse effects in patients using a bismuth colloidal pectin granules quadruple therapy.

NCT ID: NCT04636866 Completed - Clinical trials for Helicobacter Pylori Infection

The Prevalence of Helicobacter Pylori in Shanghai, 2013 to 2019

Start date: February 10, 2020
Phase:
Study type: Observational

The study was a cross-sectional single-center study, conducted at Renji Hospital, Shanghai Jiaotong university school of medicine. We retrieved the medical records of all patients who had undergone upper gastrointestinal endoscopy from January 1, 2013 through December 31, 2019. The medical records were analyzed for the prevalence of H. pylori infection in patients with peptic ulcers.

NCT ID: NCT04621487 Completed - Clinical trials for Helicobacter Pylori Infection

Quadruple vs Tailored Therapy in the Treatment of Helicobacter Pylori Infection

Start date: January 15, 2019
Phase: N/A
Study type: Interventional

Non-bismuth quadruple therapies have been proposed as potential strategies in improving the efficacy of first-line treatments. The non-bismuth quadruple therapy in its concomitant variant consists of proton pump inhibitor, amoxicillin, nitroimidazole and clarithromycin given concurrently twice daily. As a result of concurrent administration this therapy has given better results according to some studies in comparison to sequential variants. However, this therapy, as well suffers from the aforementioned increase in antibiotic resistance. Therefore, the aim of this study was to compare concomitant non-bismuth quadruple therapy with a tailored therapy based on antibiotic strain susceptibility testing.

NCT ID: NCT04617613 Completed - Clinical trials for Helicobacter Pylori Infection

Comparing Different Regimens for Eradication of Helicobacter Pylori in Kuwait

Start date: September 2016
Phase: Phase 4
Study type: Interventional

Eradication of H. pylori reduces morbidity in patients with chronic gastritis and can prevent gastric cancer. We aimed to evaluate the efficacy of clarithromycin-based triple therapy and non-bismuth based quadruple therapy for eradicating H. pylori in patients with chronic gastritis in Kuwait.

NCT ID: NCT04531059 Completed - Clinical trials for Helicobacter Pylori Infection

Rescue Therapy for Helicobacter Pylori Eradication

Start date: October 15, 2020
Phase: Phase 4
Study type: Interventional

Current guidelines have recommended classical bismuth-containing quadruple therapy including proton-pump inhibitor, bismuth, tetracycline, metronidazole as the empirical rescue therapy. However, tetracycline is clinically unavailable in China and the high frequency of adverse events of bismuth quadruple therapy often result in poor compliance, which limited the applicability of this recommendation. This study aimed to compare the efficacy and tolerability of a 14-day bismuth-containing quadruple rescue therapy in which tetracycline was replaced by minocycline.