simethicone and Gastroesophageal-Reflux

simethicone has been researched along with Gastroesophageal-Reflux* in 5 studies

Reviews

1 review(s) available for simethicone and Gastroesophageal-Reflux

ArticleYear
[Gastroesophageal reflux disease: pathogenesis, clinical manifestation, diagnostics, and treatment].
    Klinicheskaia meditsina, 2005, Volume: 83, Issue:9

    Topics: Aluminum Hydroxide; Antacids; Anti-Ulcer Agents; Antifoaming Agents; Drug Combinations; Gastroesophageal Reflux; Gastroscopy; Humans; Magnesium Hydroxide; Ranitidine; Simethicone

2005

Trials

4 trial(s) available for simethicone and Gastroesophageal-Reflux

ArticleYear
Effect of magnesium alginate plus simethicone on gastroesophageal reflux in infants.
    Journal of pediatric gastroenterology and nutrition, 2015, Volume: 60, Issue:2

    Gastroesophageal reflux (GER) is a frequently occurring condition in infants capable of causing distressing symptoms. The aim of our study is to evaluate the efficacy of Mg alginate plus simethicone (Gastrotuss Baby, DMG Italia SRL, Pomezia, Italy), compared with rice-starch-thickened formula or with reassurance alone, in the treatment of GER in infants.. The present randomized controlled trial was conducted in full-term infants affected by symptoms suggestive of GER, evaluated through a validated questionnaire (Infant Gastroesophageal Reflux Questionnaire Revised). The patients were randomized into 3 groups according to treatment (group A: Mg alginate plus simethicone; group B: thickened formula; group C: reassurance with lifestyle changes). Evaluation of symptom scores was performed after 1 month (T1) and 2 months (T2).. A total of 64 (85.3%) of 75 enrolled infants (median age 5 months; range 1-10) concluded the study. After 1 month of treatment (T1), infants treated with Mg alginate plus simethicone showed a statistically significant improvement in symptoms compared with the thickened formula and reassurance (P < 0.03, <0.0001, respectively). At the end of the study, all 3 groups of patients showed a significant reduction in symptom scores (P < 0.002, <0.038, <0.03, respectively). Median symptom score values were more significantly reduced in group A than in group B and in group C (group A vs group B P < 0.002; group A vs group C P < 0.0001; group B vs group C P < 0.001).. Mg alginate plus simethicone seems to be more efficacious on GER symptom scores than thickened formula and reassurance with lifestyle changes alone.

    Topics: Alginates; Antifoaming Agents; Drug Therapy, Combination; Female; Gastroesophageal Reflux; Glucuronic Acid; Hexuronic Acids; Humans; Infant; Infant Formula; Life Style; Male; Prospective Studies; Severity of Illness Index; Simethicone; Surveys and Questionnaires

2015
Multicenter, randomized, double-blind study comparing 20 and 40 mg of pantoprazole for symptom relief in adolescents (12 to 16 years of age) with gastroesophageal reflux disease (GERD).
    Clinical pediatrics, 2006, Volume: 45, Issue:8

    An age-appropriate questionnaire (GASP-Q) was used to assess the frequency and severity of the gastroesophageal reflux disease (GERD) symptoms: abdominal/belly pain, chest pain/heartburn, pain after eating, nausea, burping/belching, vomiting/regurgitation, choking when eating, and difficulty swallowing, in adolescents age 12 to 16 years. The primary objective was to compare the mean composite symptom score (CSS) at week 8 with baseline after treatment with 20 or 40 mg of pantoprazole. Statistically significant (p < 0.001) improvement in CSS occurred in both groups. Safety was comparable between the 2 groups. Pantoprazole was safe, well tolerated, and effective in reducing symptoms of GERD in adolescents.

    Topics: 2-Pyridinylmethylsulfinylbenzimidazoles; Adolescent; Aluminum Hydroxide; Antacids; Anti-Ulcer Agents; Child; Double-Blind Method; Drug Combinations; Female; Gastroesophageal Reflux; Humans; Magnesium Hydroxide; Male; Pantoprazole; Simethicone; Surveys and Questionnaires

2006
[A new granular effervescent 10-mg formulation of cisapride in the treatment of gastroesophageal reflux].
    La Clinica terapeutica, 1993, Volume: 142, Issue:2

    The efficacy and tolerability of Cisapride effervescent granules for treatment of gastroesophageal reflux disease were compared to a metoclopramide-dimeticone combination. The double-blind study was performed in two groups of 10 patients each who received 3 sachets daily of either drug for 8 weeks. Cisapride effervescent granules induced a statistically significant improvement of 75% of symptoms (6/8) while this improvement was obtained with the reference drug for only 60% (3/5). Statistical evaluation showed Cisapride effervescent granules to be more effective than the reference drug for 2 of 5 evaluable symptoms; mean global improvement amounted to 83 vs 58%. Final physician opinion was more favorable to Cisapride effervescent granules than to the reference drug (p < 0.005). Treatment did not have to be withdrawn nor were clinically significant changes of laboratory values observed. Both drugs were found to be well tolerated without differences between the two groups. Three patients treated with Cisapride effervescent granules complained of short-lasting mild abdominal discomfort the relations of which to the drug was doubtful, and which subsided spontaneously without need to withdraw treatment or to apply other types of therapy.

    Topics: Adult; Aged; Cisapride; Double-Blind Method; Drug Combinations; Drug Tolerance; Female; Gastroesophageal Reflux; Humans; Male; Metoclopramide; Middle Aged; Piperidines; Powders; Serotonin Antagonists; Simethicone; Time Factors

1993
Ranitidine, cimetidine, antacids, and gastro-oesophageal reflux: results of a 20-hour oesophageal pH study.
    International journal of clinical pharmacology research, 1984, Volume: 4, Issue:3

    This study compared the effects of cimetidine, ranitidine, and antacids on oesophageal pH levels. Forty-five patients were confirmed as having a gastro-oesophageal acid reflux by 3-hour postprandial metered pH measurements. The 45 patients were randomly placed into three treatment groups; one group received cimetidine 1 g/day, the second received ranitidine 300 mg/day, and the third received 60 ml/day of an antacid. The patients were retested under treatment (3-hour postprandial metered pH and prolonged 20-hour metered pH). The 3-hour postprandial metered pH was then compared to the pretreatment tests. The 20-hour postprandial metered pH test was compared with the results from 43 control (untreated) subjects with gastro-oesophageal acid refluxes. The 3-hour postprandial comparison showed a significant decrease in acid reflux with all three treatment drugs. The 20-hour measurement demonstrated a significant decrease with all three drugs in the number of acid reflux incidences compared to the untreated control patients; the ranitidine group had a significant decrease in the percentage of time with acid pH. No significant differences appeared in the comparison of the records of the 45 treated patients except for the percentage of time below pH 2 for 20 hours which was significantly lower for ranitidine. All three treatments were effective with a clear advantage in favour of ranitidine.

    Topics: Adult; Aged; Aluminum Hydroxide; Antacids; Cimetidine; Esophagus; Female; Gastroesophageal Reflux; Humans; Hydrogen-Ion Concentration; Magnesium Hydroxide; Male; Middle Aged; Monitoring, Physiologic; Random Allocation; Ranitidine; Simethicone

1984