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Clinical Trial Summary

Chinese patients who require gastrointestinal endoscopy will receive an intra-gastric single dose of NPO-11 20ml. The superiority of NPO-11 compared to placebo as a premedication for endoscopy will be verified in a randomized, double-blind, parallel-assignment design based on the proportion of patients having no gastric peristalsis.

The safety of NPO-11 will be evaluated based on adverse events and adverse drug reactions observed between informed consent and 7 days after administration in comparison with the placebo group.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Patients Undergoing Gastrointestinal Endoscopy

NCT number NCT03263910
Study type Interventional
Source Nihon Pharmaceutical Co., Ltd
Contact
Status Completed
Phase Phase 3
Start date August 21, 2017
Completion date August 17, 2018