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NCT Number: NCT00973206

Factors Influencing Cardiovascular Prognosis

The purpose of this study is to identify risks for cardiovascular events in a follow up period of 10 years.

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Observational

About this study

Inclusion criteria

  • Age > 50 years volunteers (2 towns of 15000 residents one in the north and one in the south of Greece)
  • End points
  • 5-10 years cardiovascular morbidity and mortality

Measurements at baseline

  • Anthropometrics
  • Age (M>55 years; W>65 years)
  • Weight-height- BMI
  • Abdominal obesity (Waist circumference>102 cm(M), >88cm (W) Family history
  • Family history of premature CV disease (M at age<55 years; W at age<65 years)

History

  • Smoking
  • Diabetes Mellitus,
  • Established Heart disease: myocardial infarction; angina; coronary revascularization; heart failure
  • Established renal disease [diabetic nephropathy; renal impairment (serum creatinine M>133, W>124 mmol/l); proteinuria (> 300 mg/24 h)]
  • Cerebrovascular disease: ischaemic stroke; cerebral haemorrhage; transient ischaemic attack
  • Peripheral artery disease
  • Advanced retinopathy: haemorrhages or exudates, papilloedema
  • Treatment

Measurements

  • Measurements Blood pressure
  • Clinic BP
  • 24h ABPM
  • Home BP

Heart

  • Electrocardiographic LVH
  • Echocardiographic LVH

Vessels

  • Carotid wall thickening or plaque
  • Carotid-femoral pulse wave velocity
  • Ankle/brachial BP index

Lipids or other risk factors

  • Total cholesterol, Tg, HDL, LDL
  • Plasma creatinine, estimated glomerular filtration rate
  • Fasting plasma glucose or postload plasma glucose
  • Microalbuminuria and albumin-creatinine ratio
  • Glucose tolerance test
  • Follow up each 3 year with all the above measurements

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All age >50 volunteers

Exclusion criteria

  • None

Treatment and study plan

Primary outcomes

  1. Cardiovascular mortality

    Time frame: 10 years

Secondary outcomes

  1. Hospitalization for CV events

    Time frame: 10 years

Study contacts

Contact information is provided by the study sponsor or research team.

Vasilios Kotsis, Prof

CONTACT

[email protected]

6974748860 ext. +30

Sponsors and collaborators

Lead sponsor

Aristotle University Of Thessaloniki

Other

Registry information

Official study title

Factors Influencing Cardiovascular Prognosis in Hypertensive Patients (Pythia Study)

Acronym: Pythia-GR

Important dates

Study start
2017
Primary completion
2027
Study completion
2027
First posted
Sep 9, 2009
Registry last updated
Jun 25, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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