PREVENTION OF RELAPSE IN REFLUX ESOPHAGITIS - A PLACEBO-CONTROLLED STUDY OF RANITIDINE 150 MG BID AND 300 MG BID

Citation
Jh. Hegarty et al., PREVENTION OF RELAPSE IN REFLUX ESOPHAGITIS - A PLACEBO-CONTROLLED STUDY OF RANITIDINE 150 MG BID AND 300 MG BID, Canadian journal of gastroenterology, 11(1), 1997, pp. 83-88
Citations number
22
Categorie Soggetti
Gastroenterology & Hepatology
ISSN journal
08357900
Volume
11
Issue
1
Year of publication
1997
Pages
83 - 88
Database
ISI
SICI code
0835-7900(1997)11:1<83:PORIRE>2.0.ZU;2-D
Abstract
OBJECTIVE: To compare the efficacy and safety of long term use of rani tidine 150 mg bid, 300 mg bid and placebo in prevention of endoscopic and symptomatic relapse of reflux esophagitis in an international, dou ble-blind, placebo controlled, parallel group study. PATIENTS AND METH ODS: A total of 279 patients at least 18 years old from hospital out-p atient departments with healed esophagitis (grade 0) with no or mild s ymptoms entered the study. Patients were randomly allocated to receive ranitidine 150 mg, 300 mg or placebo twice daily for 48 weeks. Patien ts returned for symptom assessments at eight-week intervals and for re -endoscopy every 16 weeks. RESULTS: Both ranitidine regimens were sign ificantly more effective than placebo in preventing endoscopic and sym ptomatic relapse of reflux esophagitis (P=0.003 for ranitidine 150 mg bid; P<0.001 for ranitidine 300 mg bid). No statistically significant differences were observed in relapse rates between the two ranitidine regimens. The percentage of patients with endoscopic relapse (grade 2) after 48 weeks were 60%, 37% and 27% for placebo, ranitidine 150 mg b id and ranitidine 300 mg bid, respectively (P=0.002 for ranitidine 150 mg bid versus placebo; P<0.001 for ranitidine 300 mg bid versus place bo). Ranitidine was well tolerated. CONCLUSIONS: Ranitidine 150 mg bid and 300 mg bid are safe and effective treatments in the prevention of reflux esophagitis relapse.