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
| Type | Name | Description |
|---|---|---|
| DRUG | Lansoprazole | Lansoprazole 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.