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Real Life Experience of the Use of Isomers as ALENCAL (Levamlodipine) for Evaluation of Efficacy, Safety and Tolerability in the Management of Cardiovascular Disease in Colombian Patients (XPRES)

C

Closter Pharma

Status

Unknown

Conditions

Hypertension

Study type

Observational

Funder types

Industry

Identifiers

NCT01429233
COL-CARDIO-NIS001

Details and patient eligibility

About

This is a Phase 4, observational, open study in patients whom their doctor for clinical practice prescribes levamlodipine. No medication was provided by the sponsor. The planned observation time is 8 weeks. The 8 weeks of observation involves an evaluation of baseline followed by information gathered from the assessment visits at week 4 and week 8, or clinical practice.

Enrollment

2,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patients whose primary physician based on their clinical condition and locally approved use will be eligible to participate in this study, and have been prescribe with Levamlodipine.

Trial contacts and locations

1

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Central trial contact

Harold Mejia; Sandra M Casiano, M.D.

Data sourced from clinicaltrials.gov

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