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Identification of Parameters in rapId-proGression Subgroup Patients With Moderate Aortic Stenosis

NCT01575249 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2012-04-11

No results posted yet for this study

Summary

The investigators aim to identify all clinical, biological, echo and imagistic parameters that predispose to increased progression rates in a prospective observational trial which will include ONLY patients with moderate AS, with the complete cardiological investigational tools provided in 2012. Once those parameters are found, medical and interventional treatment could be implemented to decrease the mortality rates.

Conditions

  • Aortic Stenosis

Sponsors & Collaborators

  • Carol Davila University of Medicine and Pharmacy

    lead OTHER

Principal Investigators

  • ALEXANDRU N MISCHIE, MD · BAGDASAR ARSENI EMERGENCY HOSPITAL

Eligibility

Min Age
50 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-07-31
Primary Completion
2016-01-31
Completion
2016-06-30

Countries

  • Romania

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01575249 on ClinicalTrials.gov