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Clinical Trials/NCT00421239
NCT00421239
Completed
Not Applicable

Retrospective Study of Hypertensive Urgencies in Patients With Arterial Hypertension

Russian Cardiology Research and Production Center1 site in 1 country1,200 target enrollmentJanuary 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertensive Urgency
Sponsor
Russian Cardiology Research and Production Center
Enrollment
1200
Locations
1
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The purpose of this study is to determine whether frequent hypertensive urgencies increase the risk of cardiovascular events in patients with arterial hypertension.

Detailed Description

The spectrum of disorders associated with arterial hypertension (AH) encompasses chronic uncomplicated hypertension and the hypertensive crises, including hypertensive urgences and emergencies. Hypertensive crises accounted for more than 25% of all patient visits to a medical section of an emergency department, with hypertensive urgences (HU) accounting for two-third of these cases. Hypertensive crises, without prompt treatment, are often associated with morbidity and mortality. We propose to conduct a population-based case-control study of HU in areas of the Russian Federation. We will include about thirty study centers and one data coordinating center and will recruit study participants over a period of one years. We plan to conduct in-person interviews with 1,500 cases and 1,500 controls to elicit information on demographic background and history of exposures. We intend to test about 20-25 risk factors of HU thus calculated target number of subject is 3000 pts. We're going to get access to hospital lists in each study center. From the database we'll select patients with AH and recruit every third participant who came to hospital or/and policlinic. Every selected participant will be asked to respond to some questions by phone and be divided into two groups. Participants who have HU two weeks before the call will be questioned about level of arterial pressure and treatment during HU. Participants with often HU (every week or more) will be included into first group (prevalent cases, group A). Participants with seldom HU (every month or less) will be included into second group (controls, group B). Cases and controls will be selected from the same population of AH patients. Questionnaire contains information about age, gender, tobacco use, data about HU (frequency, treatment and its complications), antihypertensive and concomitant treatment, level of blood pressure, regularity of taking antihypertensive drugs, associated clinical conditions (cerebrovascular disease, heart disease, renal disease, peripheral vascular disease), PCI, CABG, if it be possible we intend to collect information of factors influencing prognosis (fasting plasma glucose, dyslipidaemia, serum creatinine, serum uric acid, left ventricular hypertrophy).

Registry
clinicaltrials.gov
Start Date
January 2007
End Date
December 2008
Last Updated
17 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Russian Cardiology Research and Production Center

Eligibility Criteria

Inclusion Criteria

  • Cases: every third patient from hospital/policlinic database who are diagnosed with arterial hypertension (SBP/DBP\>140/90 Hg or taking anti hypertensive drugs) and with frequent (weekly or daily) hypertensive urgencies (SBP/DBP≥180/110 Hg) will be potentially eligible for the study.
  • Controls will be selected from the same population of participants by random telephone dialing to every third patient with arterial hypertension (SBP/DBP\>140/90 Hg or taking anti hypertensive drugs) and with seldom (monthly, several times in the year or never) hypertensive urgencies.

Exclusion Criteria

  • Hypertensive emergency

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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