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NCT00573742 Clinical Trial

Efficacy Observational Study of Candesartan Cilexetil on Hypertensive Patients

Primary Hypertension Clinical Trial

Official title:
Non-interventional Study on Uncontrolled Hypertensive Patients for Evaluating Efficacy of Candesartan Cilexetil as Monotherapy or add-on Therapy.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00573742
Other study ID # NIS-CRO-ATA-2007/1
Secondary ID
Status Completed
Phase N/A
First received December 13, 2007
Last updated August 18, 2010
Start date September 2007
Est. completion date February 2008

Study information
Verified date August 2010
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Romainia: National Drug Agency
Study type Observational

Clinical Trial Summary

The purpose of this study is to observe treatment with candesartan cilexetil 16mg for 8 weeks, in uncontrolled hypertensive patients, in improvement of achieving of treatment goals and impact on blood pressure level in patients with uncontrolled hypertension treated with candesartan cilexetil.

Recruitment information / eligibility
Status Completed
Enrollment 1940
Est. completion date February 2008
Est. primary completion date February 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- diagnosis of essential hypertension (mild or moderate as defined in European Guidelines of Hypertension, 2003), that are treated already with candesartan cilexetil 16mg o.d. within last 2 weeks or more, according to Romanian approved Atacand SPC. Written informed consent to allow access and use(analysis) of data collected

Exclusion Criteria:

- Patients not to be included in the programme: patients who have any contraindication to the product as detailed in Romanian approved Atacand SPC. Use of specific concomitant medication known to present a potential safety concern according to Romanian approved SPC

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Drug:
• Candesartan Cilexeotil 16mg

Locations
Country Name City State
Romania Research Site Bacau
Romania Research Site Braila
Romania Research Site Brasov
Romania Research Site Bucuresti
Romania Research Site Cluj
Romania Research Site Constanta
Romania Research Site Craiova
Romania Research Site Galati
Romania Research Site Ghiroda
Romania Research Site Iasi
Romania Research Site Lugoj
Romania Research Site Oradea
Romania Research Site Pitesti
Romania Research Site Ploiesti
Romania Research Site Sibiu
Romania Research Site Timisoara

Sponsors (1)
Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Romania, 

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