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Esophagitis, Peptic clinical trials

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NCT ID: NCT04034017 Completed - Clinical trials for Gastroesophageal Reflux

Gastroesophageal Reflux Disease Among College Students

Start date: September 1, 2018
Phase:
Study type: Observational

Background: Gastroesophageal reflux disease (GERD) is a worldwide prevalent gastrointestinal disorder which has negative impacts on quality of life, health and economy. The aims of this study were to assess the prevalence of GERD among college students in southwestern Saudi Arabia and to evaluate its personal, academic and stress correlates Materials and Methods: Through a cross-sectional study design, a self-reported questionnaire was distributed between a representative sample of students in health and non-health care colleges in southwestern Saudi Arabia. The questionnaire included data for personal characteristics, academic study, and Arabic versions of GERD questionnaire (GerdQ) and Cohen's Perceived Stress Scale.

NCT ID: NCT03998969 Completed - Esophageal Disease Clinical Trials

Efficacy of DA-5204 on Gastroesophageal Reflux Disease

Start date: June 1, 2016
Phase: Phase 3
Study type: Interventional

This is a single-center, randomized, double-blind, placebo-controlled clinical Study to evaluate the efficacy of DA-5204 and proton pump inhibitor combination therapy compared with proton pump inhibitor alone therapy in patients with gastroesophageal reflux Disease.

NCT ID: NCT03883074 Completed - Clinical trials for Gastro Esophageal Reflux

Effect of a Combination of Hyaluronic Acid, Chondroitin Sulphate and Magnesium Trisilicate on Subjects With GastroEsophageal Reflux Disease

Start date: December 20, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to investigate whether a 3-week treatment with an oral melt in mouth medical device, made up with hyaluronic acid, chondroitin sulphate and magnesium trisilicate, can lead to a reduction of Gastroesophageal Reflux Disease symptoms and to an improvement of the integrity of esophageal mucosa in patients who are to experiencing esophagus symptoms. The study is a randomized, double-blind cross-over placebo controlled study. Every patient will get both the active study device during one study period and placebo during another another period.

NCT ID: NCT03881722 Completed - Clinical trials for Gastro Esophageal Reflux

Effect of Magnesium Alginate in Infants With Gastroesophageal Reflux.

Start date: June 2016
Phase: Phase 3
Study type: Interventional

Recurrent regurgitation stress the infants and their parents and often results in an inappropirate use of PPI prescription in infancy. The aim of this study is to evaluate the efficacy of Mg alginate in infants with symptoms of gastroesophageal reflux.

NCT ID: NCT03871426 Completed - Clinical trials for Gastroesophageal Reflux Disease

Manual Therapy Effects on Upper and Lower Esophageal Sphincter Pressures

Start date: March 18, 2019
Phase:
Study type: Observational

The aim of this study is to test the influence of manual cervical traction and chest stabilization maneuvers on pressures in upper and lower esophageal sphincters.

NCT ID: NCT03788109 Completed - Clinical trials for Functional Dyspepsia

Relationship Between Gastric Accommodation, TLESRs and Reflux in HV and in GERD With or Without Overlapping Dyspepsia

Start date: June 12, 2018
Phase: N/A
Study type: Interventional

Our group recently studied the relationship between intra-gastric pressure (IGP) and reflux events after a meal, both in gastro-esophageal reflux disease (GERD) and in healthy volunteers (HV). Ingestion of a meal was accompanied by a drop in IGP, probably representing gastric accommodation (GA). However, the magnitude of this IGP drop varied, and was inversely correlated with the number of transient lower esophageal sphincter relaxations (TLESRs) and the number of reflux events, both in patients and in HV: a smaller meal-induced drop in IGP was associated with a higher rate of reflux events, and vice versa. These findings suggest that impaired GA is a trigger for reflux. Furthermore, impaired GA is a well-established mechanism underlying symptom generation in functional dyspepsia (FD). Hence, the investigators hypothesize that impaired GA is an important pathophysiological feature explaining the overlap between GERD and FD. To evaluate this hypothesis, the investigators will study the relationship between GA, TLESRs and reflux events in HV and in a group of GERD patients which will be categorized as pure GERD or GERD/FD overlap.

NCT ID: NCT03777787 Completed - Clinical trials for Gastro Esophageal Reflux

Bitter Tastants and Reflux

Start date: January 14, 2019
Phase: N/A
Study type: Interventional

Recently the relationship between intragastric pressure (IGP) and reflux events after a meal was investigated, both in gastro-esophageal reflux disease (GERD) patients and in healthy volunteers. Ingestion of a meal was accompanied by a drop in IGP. However, the magnitude of this drop varied and was inversely correlated with the number of transient lower esophageal sphincter relaxations (TLESRs) and the number of reflux events, both in patients and in healthy volunteers: a smaller meal-induced drop in IGP was associated with a higher rate of reflux events and vice versa. This finding suggests that a smaller meal-induced drop may act as a trigger for reflux. It has been demonstrated that bitter administration leads to a smaller meal-induced drop. Therefore, bitter can be a dietary trigger for TLESRs facilitating the occurrence of symptoms of GERD. To evaluate this hypothesis, the researchers will study the relationship between bitter and the occurrence of TLESRs and reflux events in healthy volunteers. Additionally, it has been demonstrated that administering bitter also influences the concentration of motilin. Therefore, the research team will also measure the concentration of motilin to investigate whether changes in motilin concentrations can influence the number of TLESRs, via a change in gastric tone.

NCT ID: NCT03735862 Completed - Clinical trials for Gastroesophageal Reflux

Complications, Outcomes and Revisions Following Hiatal Hernia Repair With MIROMESH

Start date: June 1, 2017
Phase:
Study type: Observational

Investigator will identify a consecutive cohort of patients who have undergone a hiatal hernia repair and are at least 6 months post index procedure.

NCT ID: NCT03619811 Completed - Clinical trials for Gastroesophageal Reflux

Precision Approach to PPI Therapy in Gastroesophageal Reflux Disease

Start date: July 13, 2018
Phase: N/A
Study type: Interventional

This study plans to learn more about reflux associated laryngeal symptoms, and more efficient ways to diagnose and treat this condition.

NCT ID: NCT03616119 Completed - Clinical trials for Gastroesophageal Reflux Disease

Gastroesophageal Reflux Disease in Azerbaijan

Start date: January 1, 2018
Phase:
Study type: Observational [Patient Registry]

To evaluate the prevalence of Gastroesophageal reflux disease in Azerbaijan. It is intended to evaluate the prevalence of the disease in the regions as well as the capital by cluster sampling ,ethitology and to compare the outcomes depending on the geographical location.