A double-blind randomized study comparing different dose regimens of H2-receptor antagonists on 24-hour gastric secretion in normal subjects and duodenal ulcer patients

Am J Gastroenterol. 1987 Jan;82(1):36-41.


Duodenal ulcer therapy with H2 antagonists initially aimed to control acid secretion throughout the 24-h period, but recently nighttime suppression has been advocated. The effect of single nighttime regimens of cimetidine 400 mg BID, cimetidine 800 mg HS, ranitidine 150 mg HS, and placebo on 24-h intragastric acidity, nocturnal acid output, and pepsin secretion were studied in four healthy volunteers and four patients with healed duodenal ulcer. A nonrandomized dose of cimetidine 1200 mg HS was also studied. For all four treatments, daytime (0730-2230 h) intragastric acidity was reduced by 4-30% in the normals and by 10-44% in the duodenal ulcer patients (NS), while 24-h intragastric acidity was reduced by 44-46% and 40-64%, respectively (p less than 0.05). Reduction in nocturnal acid output was 82-96% in normals and 91-99% in duodenal ulcer, respectively. Pepsin concentration was unaffected by treatment but pepsin concentration was significantly (p less than 0.05) lower in patients than in normals. Mean 24-h gastric acid secretion was reduced by a single nighttime treatment with an H2-receptor antagonist, while nocturnal acid secretion was virtually abolished. H2 antagonists given only at night deserve further clinical evaluation to determine the minimal effective dose and optimal duration of suppression to achieve ulcer healing.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Cimetidine / administration & dosage*
  • Cimetidine / pharmacology
  • Circadian Rhythm
  • Clinical Trials as Topic
  • Double-Blind Method
  • Drug Administration Schedule
  • Duodenal Ulcer / blood
  • Duodenal Ulcer / physiopathology*
  • Gastric Acid / metabolism*
  • Gastrins / blood
  • Humans
  • Pepsin A / metabolism
  • Prolactin / blood
  • Random Allocation
  • Ranitidine / administration & dosage*
  • Ranitidine / pharmacology


  • Gastrins
  • Cimetidine
  • Ranitidine
  • Prolactin
  • Pepsin A