Candesartan Cilexetil/Amlodipine Besilate Combination Tablets LD, HD Special Drug Use Surveillance "Hypertension: Long-Term Use"

NCT02068495 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3409

Last updated 2018-07-26

Study results available
· View outcomes & findings →

Summary

The purpose of this survey is to investigate the safety and efficacy of long-term use of candesartan cilexetil/amlodipine besilate combination tablets (Unisia Combination Tablets) low dose (LD), high dose (HD) in participants with hypertension in the normal clinical setting.

Conditions

Interventions

DRUG

Candesartan cilexetil/Amlodipine besilate

Candesartan cilexetil/Amlodipine besilate tablets

Sponsors & Collaborators

Principal Investigators

  • Study Director · Takeda

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-06-15
Primary Completion
2013-05-31
Completion
2013-05-31

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02068495 on ClinicalTrials.gov