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Clinical effectiveness of a new antacid chewing gum on heartburn and oesophageal pH control.

AbstractBACKGROUND:
Oesophageal acid neutralization with antacids depends on the duration of oesophageal antacid exposure and acid neutralizing capacity. A gum that releases antacid as it is chewed could take advantage of both mechanisms to enhance heartburn relief.
METHODS:
Twenty-four subjects were crossed over to four regimens: placebo, chewable antacid tablets (1000 mg CaCO3), lower dose gum (600 mg CaCO3) and higher dose gum (900 mg CaCO3). A dual pH probe was placed, subjects ate a standardized provocative meal and self-dosed once as needed. Symptoms were recorded every 15 min using visual analogue and Likert scales.
RESULTS:
SYMPTOMS:
Both gums decreased heartburn compared to placebo for 120 min. Higher dose gum decreased heartburn more than chewable antacids up to 120 min post-dose. pH: Active chewable antacid and gums immediately increased oesophageal pH, with significant improvement 15-30 min post-dose.
SUMMARY:
(i) both gums promptly decreased heartburn and elevated oesophageal pH; (ii) both gums provided sustained relief for 120 min; (iii) antacid gums provided faster and more prolonged symptom relief and pH control than chewable antacids.
CONCLUSIONS:
Calcium carbonate gum effectively neutralizes oesophageal acidity and relieves symptoms following a meal, and is superior to chewable antacids in terms of the duration of heartburn relief.
AuthorsK L Collings, S Rodriguez-Stanley, H M Proskin, M Robinson, P B Miner Jr
JournalAlimentary pharmacology & therapeutics (Aliment Pharmacol Ther) Vol. 16 Issue 12 Pg. 2029-35 (Dec 2002) ISSN: 0269-2813 [Print] England
PMID12452946 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
Chemical References
  • Antacids
  • Chewing Gum
  • Delayed-Action Preparations
  • Calcium Carbonate
Topics
  • Adolescent
  • Adult
  • Antacids (administration & dosage)
  • Calcium Carbonate (administration & dosage)
  • Chewing Gum
  • Cross-Over Studies
  • Delayed-Action Preparations
  • Dose-Response Relationship, Drug
  • Esophagus (metabolism)
  • Gastric Acidity Determination
  • Gastric Mucosa (metabolism)
  • Heartburn (drug therapy, metabolism)
  • Humans
  • Hydrogen-Ion Concentration (drug effects)
  • Male
  • Middle Aged
  • Severity of Illness Index
  • Single-Blind Method

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