A placebo-controlled dose-ranging study of lansoprazole in the management of reflux esophagitis
- PMID: 9468251
- DOI: 10.1111/j.1572-0241.1998.00238.x
A placebo-controlled dose-ranging study of lansoprazole in the management of reflux esophagitis
Abstract
Objective: We compared the efficacy of three different doses of the proton pump inhibitor lansoprazole in the management of reflux esophagitis.
Methods: Two hundred ninety-two patients with endoscopically confirmed reflux esophagitis were enrolled in a double-blind, multicenter study and were randomized to lansoprazole 15, 30, or 60 mg or placebo administered once daily for 8 wk.
Results: Healing rates after 4 wk of lansoprazole 15, 30, and 60 mg/d were 67.6%, 81.3%, and 80.6%, respectively. These were all significantly superior (p < 0.001) to placebo, which produced endoscopic healing in only 32.8% of the patients after 4 wk. The 4-wk healing rates with lansoprazole 30 or 60 mg were significantly higher than that with lansoprazole 15 mg (p < 0.05), confirming a dose-response effect. Cumulative healing rates after 8 wk of treatment were 52.5% with placebo and 90.0%, 95.4%, and 94.4% with lansoprazole 15, 30, and 60 mg, respectively (p < 0.001 for all doses of lansoprazole vs placebo). Lansoprazole was also significantly superior to placebo in relieving symptoms in patients with reflux esophagitis. Lansoprazole was well tolerated, and no serious treatment-related adverse events were encountered. Up to 3 months after discontinuation of treatment, all lansoprazole-treated groups had more patients free of endoscopic evidence of esophagitis than the group treated with placebo.
Conclusions: Lansoprazole was safe and effective for the treatment of reflux esophagitis in this trial. This study indicates that the optimum daily dose of lansoprazole for reflux esophagitis is 30 mg.
Similar articles
-
Efficacy and safety of lansoprazole in the treatment of erosive reflux esophagitis. The Lansoprazole Group.Am J Gastroenterol. 1996 Sep;91(9):1749-57. Am J Gastroenterol. 1996. PMID: 8792693 Clinical Trial.
-
Lansoprazole heals erosive reflux esophagitis resistant to histamine H2-receptor antagonist therapy.Am J Gastroenterol. 1997 Mar;92(3):429-37. Am J Gastroenterol. 1997. PMID: 9068463 Clinical Trial.
-
Treatment of reflux esophagitis resistant to H2-receptor antagonists with lansoprazole, a new H+/K(+)-ATPase inhibitor: a controlled, double-blind study. Lansoprazole Study Group.Am J Gastroenterol. 1993 Aug;88(8):1212-7. Am J Gastroenterol. 1993. PMID: 8101695 Clinical Trial.
-
Treatment of gastroesophageal (acid) reflux with lansoprazole: an overview.Clin Ther. 1993;15 Suppl B:2-13. Clin Ther. 1993. PMID: 7911400 Review.
-
[Lansoprazole--profile of a new proton pump inhibitor].Leber Magen Darm. 1994 Mar;24(2):66-8, 71. Leber Magen Darm. 1994. PMID: 8196467 Review. German.
Cited by
-
Efficacy and safety of proton pump inhibitors versus vonoprazan in treatment of erosive esophagitis: A PRISMA-compliant systematic review and network meta-analysis.Medicine (Baltimore). 2022 Nov 25;101(47):e31807. doi: 10.1097/MD.0000000000031807. Medicine (Baltimore). 2022. PMID: 36451489 Free PMC article.
-
Prevalence of complicated gastroesophageal reflux disease and Barrett's esophagus among racial groups in a multi-center consortium.Dig Dis Sci. 2009 May;54(5):964-71. doi: 10.1007/s10620-009-0742-3. Epub 2009 Mar 3. Dig Dis Sci. 2009. PMID: 19255852 Free PMC article.
-
Deprescribing versus continuation of chronic proton pump inhibitor use in adults.Cochrane Database Syst Rev. 2017 Mar 16;3(3):CD011969. doi: 10.1002/14651858.CD011969.pub2. Cochrane Database Syst Rev. 2017. PMID: 28301676 Free PMC article.
-
A systematic review of symptomatic outcomes used in oesophagitis drug therapy trials.Gut. 2004 May;53 Suppl 4(Suppl 4):iv58-65. doi: 10.1136/gut.2003.034371. Gut. 2004. PMID: 15082617 Free PMC article.
-
Lansoprazole for maintenance of remission of erosive oesophagitis.Drugs. 2002;62(8):1173-84. doi: 10.2165/00003495-200262080-00004. Drugs. 2002. PMID: 12010078 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources