TY - JOUR
T1 - Absence of symptomatic benefit of lansoprazole, clarithromycin, and amoxicillin triple therapy in eradication of Helicobacter pylori positive, functional (nonulcer) dyspepsia
AU - Van Zanten, Sander Veldhuyzen
AU - Fedorak, Richard N.
AU - Lambert, Jean
AU - Cohen, Lawrence
AU - Vanjaka, Anita
N1 - Funding Information:
This study was supported by Abbott Laboratories, Canada. We acknowledge the following contributors to the study: André Archambault, John Axler, Robert Bailey, Alan Barkun, Marc Bradette, Naoki Chiba, Lawrence Cohen, Chrystian Dallaire, Jocelyn Deneault, Gerard Duffy, Carlo Fallone, Richard Fedorak, Nanda Gopinath, Raymond Lahaie, Maynard Luterman, Norman Marcon, Eldon Shaffer, Daniel Shu, Gervais Tougas, Alain Watier, Alain Weiss, Stephen Wolman, and Lawrence Worobetz.
PY - 2003/9/1
Y1 - 2003/9/1
N2 - OBJECTIVES: The aim of this study was to compare the effect of a combination of lansoprazole, clarithromycin, and amoxicillin (LCA) versus placebo on the severity of symptoms in functional dyspepsia patients who were positive for Helicobacter pylori (H. pylori). METHODS: This was a double-blind, randomized, controlled clinical trial in adult patients with functional dyspepsia who were H. pylori positive. Patients were randomized to 7-day treatment with LCA or identical looking placebo. H. pylori status was confirmed by the urea breath test performed at baseline, at 6 wk, and at 6 and 12 months. The severity of eight upper GI symptoms was measured on a five-point Likert scale. The main outcomes were the change in average severity of the dyspepsia summary score of the eight symptoms and the proportion of patients who improved ≥4 points on the dyspepsia summary score. RESULTS: A total of 157 patients were included in the intention-to-treat analysis. LCA achieved cure of H. pylori infection in 82% of patients compared to 6% in the placebo group. The severity of dyspepsia symptoms improved over the 12-month study period, but for none of the outcome measures was there a significant difference between LCA and placebo. CONCLUSIONS: There was no difference in sustained improvement of dyspepsia symptoms when LCA was compared with placebo. An 82% cure rate of H. pylori infection was observed with LAC.
AB - OBJECTIVES: The aim of this study was to compare the effect of a combination of lansoprazole, clarithromycin, and amoxicillin (LCA) versus placebo on the severity of symptoms in functional dyspepsia patients who were positive for Helicobacter pylori (H. pylori). METHODS: This was a double-blind, randomized, controlled clinical trial in adult patients with functional dyspepsia who were H. pylori positive. Patients were randomized to 7-day treatment with LCA or identical looking placebo. H. pylori status was confirmed by the urea breath test performed at baseline, at 6 wk, and at 6 and 12 months. The severity of eight upper GI symptoms was measured on a five-point Likert scale. The main outcomes were the change in average severity of the dyspepsia summary score of the eight symptoms and the proportion of patients who improved ≥4 points on the dyspepsia summary score. RESULTS: A total of 157 patients were included in the intention-to-treat analysis. LCA achieved cure of H. pylori infection in 82% of patients compared to 6% in the placebo group. The severity of dyspepsia symptoms improved over the 12-month study period, but for none of the outcome measures was there a significant difference between LCA and placebo. CONCLUSIONS: There was no difference in sustained improvement of dyspepsia symptoms when LCA was compared with placebo. An 82% cure rate of H. pylori infection was observed with LAC.
UR - http://www.scopus.com/inward/record.url?scp=0141459714&partnerID=8YFLogxK
U2 - 10.1111/j.1572-0241.2003.07583.x
DO - 10.1111/j.1572-0241.2003.07583.x
M3 - Article
C2 - 14499772
AN - SCOPUS:0141459714
SN - 0002-9270
VL - 98
SP - 1963
EP - 1969
JO - American Journal of Gastroenterology
JF - American Journal of Gastroenterology
IS - 9
ER -