Clinical Trials Directory

Trials / Completed

CompletedNCT02099682

Long-term Use of Takepron Capsules on the Prevention of Recurrence of Gastric/Duodenal Ulcer in Patients Receiving Low-dose Aspirin

Takepron Capsules 15/ Orally Dispersing (OD) Tablets 15 Special Drug Use Surveillance Long-term Use Survey on the Prevention of Recurrence of Gastric/Duodenal Ulcer in Patients Receiving Low-dose Aspirin

Status
Completed
Phase
Study type
Observational
Enrollment
3,366 (actual)
Sponsor
Takeda · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The purpose of this study is to investigate the safety and efficacy of long-term administration of lansoprazole (Takepron) for up to 12 months in the routine clinical setting in patients receiving low-dose aspirin

Detailed description

This is a special survey on long-term use (for up to 12 months) of lansoprazole (Takepron) to determine the incidence of adverse drug reactions in the routine clinical setting in patients receiving low-dose aspirin. The usual adult dosage is 15 mg of lansoprazole administered orally once daily.

Conditions

Interventions

TypeNameDescription
DRUGLansoprazoleLansoprazole Capsules 15/ OD Tablets

Timeline

Start date
2010-08-01
Primary completion
2014-01-01
Completion
2014-01-01
First posted
2014-03-31
Last updated
2016-11-04
Results posted
2015-06-25

Source: ClinicalTrials.gov record NCT02099682. Inclusion in this directory is not an endorsement.