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Helicobacter Pylori Infection clinical trials

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NCT ID: NCT04039412 Completed - Clinical trials for Helicobacter Pylori Infection

Comparison Between Quadruple Regimens for Helicobacter Pylori Infection in Egypt

Start date: June 1, 2018
Phase: Phase 4
Study type: Interventional

The overall prevalence of H. Pylori in the developing countries is 50.8%, with the highest one presented in Africa (79.1%). Hybrid therapy is supposed to be more effective as a first-line regimen for Helicobacter pylori infection in Egypt than the Reverse hybrid and non-bismuth Levofloxacin quadruple therapies. We are aiming here to compare the Hybrid, Reverse hybrid, and Levofloxacin quadruple therapies as first-line therapy, trying to reach the safest, cost-effective, and compliance-inducing regimen in Egypt. We will conduct a randomized controlled (interventional) study at Zagazig University Hospital, internal medicine department clinic, on 330 patients. 110 patients will be allocated to each regimen.

NCT ID: NCT04037904 Completed - Clinical trials for Helicobacter Pylori Infection

Long-term Follow-up of Interleukin-1B and H+,K+-ATPase mRNA Expression After Helicobacter Pylori Eradication

Start date: February 2006
Phase:
Study type: Observational

We will evaluate the long-term changes of gastric H+, K+-adenosine triphosphatase (H+, K+-ATPase) and Interleukin-1B mRNA expression according to Helicobacter pylori (H.pylori) infection and intestinal metaplasia and investigate the long-term effect of H. pylori eradication

NCT ID: NCT04025983 Terminated - Clinical trials for Helicobacter Pylori Infection

Effectiveness of GastimunHp Plus in Supporting the Treatment of Peptic Ulcer Disease With Helicobacter Pylori Infection

GasHp
Start date: November 1, 2019
Phase: N/A
Study type: Interventional

Challenges in the treatment of Helicobacter pylori (H. pylori) include increasing antimicrobial resistance and patient's low tolerance to some regimens. Lactobacillus johnsonii (L. johnsonii) and Immunoglobulin Y (IgY) have been shown to decrease the amount and activity of H. pylori in human stomach and can increase patient's tolerance. We conduct a single-center double-masked randomized controlled trial to evaluate the effectiveness of GastimunHp Plus (a product combining L. johnsonii and IgY) in improving the clearance of H. pylori after six to eight weeks of treatment and side effects of H. pylori treatment. H. pylori is tested by C13- or C14-urea breath test.

NCT ID: NCT04024527 Completed - Clinical trials for Helicobacter Pylori Infection

High Dose of Dual Therapy Plus Metronidazole for Helicobacter Pylori RescueTreatment

Start date: July 25, 2019
Phase: Phase 4
Study type: Interventional

Dual therapy containing high dose of proton pump inhibitor (PPI) and amoxicillin had showed excellent eradication results with Helicobacter pylori first-line treatment. However, no study has examined the the efficacy of high dose of dual therapy or dual therapy plus metronidazole for H. pylori rescue treatment.This study is designed to evaluate the efficacy and safety of the addition of metronidazole to high dose of dual therapy for H. pylori rescue treatment.

NCT ID: NCT04006340 Enrolling by invitation - Clinical trials for Helicobacter Pylori Infection

Empirical vs Tailored Therapy for H. Pylori Infection

Start date: January 4, 2019
Phase: N/A
Study type: Interventional

We aimed to compare the efficacy of genotypic resistance-guided tailored therapy vs empirical therapy for eradication of Helicobacter pylori (H. pylori) infection in randomized controlled trials.

NCT ID: NCT04000243 Completed - Clinical trials for Helicobacter Pylori Infection

Diagnosis of Helicobacter Pylori Based on Gastric Collecting Venules

Start date: July 1, 2019
Phase:
Study type: Observational

Helicobacter pylori (Hp) is the major cause of gastritis and gastritis-associated diseases. Detection of a regular arrangement of collecting venules (RAC) pattern in the lesser gastric curvature correlates with negative Hp status with a sensitivity and negative predictive value (NPV) higher than 90% in Asian countries. In a recent study carried out in our hospital, it has been shown that the presence of RAC pattern in the lesser gastric curvature, evaluated with high definition endoscopy, can accurately identify patients without Hp. The aim of this study is to confirm the validity of the endoscopic diagnosis of Hp infection in the West by means of the RAC pattern in a multicenter prospective study and to evaluate interobserver variability before establishing its applicability in clinical practice.

NCT ID: NCT03997279 Not yet recruiting - Clinical trials for Helicobacter Pylori Infection

Assesment of the Efficiency and Safety Helicobacter Pylori Therapy With or Without Saccharomyces Boulardii

Start date: June 2019
Phase: Phase 4
Study type: Interventional

This study assesses the effect of quadruple therapy for H. pylori, with the addition of probiotics Saccharomyces boulardii. In addition, he assesses whether this combination reduces the frequency of adverse effects of eradication therapy, and whether it affects the compliance.

NCT ID: NCT03976739 Completed - Gastric Cancer Clinical Trials

Study on the Effect of Bile Reflux on Gastric Cancer and Its Precancerous Lesions: a Cross-sectional Study.

Start date: June 17, 2019
Phase:
Study type: Observational

To explore the effects of bile reflux on gastric cancer and its precancerous lesions, so as to better prevent the occurrence and development of gastric cancer.

NCT ID: NCT03973242 Recruiting - Clinical trials for Helicobacter Pylori Infection

Dual-focus Magnification With Narrow-band Imaging in Helicobacter Pylori Infection

Start date: March 15, 2018
Phase: N/A
Study type: Interventional

Dual-focus with narrow-band imaging (DF-NBI) is a novel technique to improve the quality of images of the irregular mucosal structures and microvessels of gastric neoplasms. The investigators compare this technique with conventional white light (WL) endoscopy to predict Helicobacter pylori infection.

NCT ID: NCT03968302 Completed - Clinical trials for Helicobacter Pylori Infection

ADDITION OF BISMUTH TO THE STANDARD TRIPLE THERAPY FOR HELICOBACTER PYLORI ERADICATION

Start date: June 1, 2018
Phase: Phase 2
Study type: Interventional

H pylori is an important cause of chronic gastritis and other complications. There is a decline in eradication rate for H pylori owing to multiple factors including drug resistance. We compare the effect of the addition of bismuth to the standard triple therapy in a randomized control trial. Subjects were randomized into two arms. Arm A received triple therapy including amoxicillin, clarithromycin, and omeprazole and Arm B received quadruple therapy adding colloidal bismuth subcitrate. Both arms received treatment for two weeks.