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COMPLETEDPhase 4NCT00819104

A Study to Compare the Efficacy, Safety and Tolerability of Selomax With Its Individual Components

This is a randomised, open-label; parallel group, multicentric study comparing the efficacy and safety of fixed-dose-combinations of Metoprolol XL plus Amlodipine with individual components of the com...

Lead sponsor: AstraZeneca•11 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

AstraZeneca

Collaborators

St. John's Research Institute

Age

18 - 80 years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Patients of hypertension (primary) , as judged by 2 BP measurements before randomisation
•Those who have given their written consent for the study.

Exclusion Criteria

•Patients of other forms of hypertension (other than primary)
•Those who have consistently BP \> /=180/120mmHg
•Patients with a prior history of chest pain, heart attacks, conduction defects and strokes.
•Patients of diabetes requiring insulin,asthma and kidney diseases.

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: September 9, 2009Terms

Trial snapshot

StatusCOMPLETED

PhasePHASE4

Enrollment402

Start dateNov 2008

Last updatedSep 9, 2009

Condition

Primary Hypertension

Locations shown

Research Site

Hyderabad, Andhra Pradesh

Research Site

Ahmedabad, Gujarat

Research Site

Bangalore, Karnataka

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: September 9, 2009Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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