Institutional Registry of Thromboembolic Disease

NCT01372514 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 4500

Last updated 2019-08-13

No results posted yet for this study

Summary

The purpose of this study is to create an institutional registry of Thromboembolic disease through a prospective survey based on epidemiological data, risk factors, diagnosis, prognosis, treatment, monitoring and survival.

The main goal is to describe the occurrence of thromboembolic disease and the characteristics of clinical presentation, evolution and predisposing factors of these episodes in the population of the Hospital Italiano de Buenos Aires.

Conditions

Sponsors & Collaborators

  • Hospital Italiano de Buenos Aires

    lead OTHER

Principal Investigators

  • Diego H Giunta, MD · Internal Medicine Clinical research Area Coordinator

  • Fernan Gonzales Bernaldo de Quirós, MD · Internal Medicine Clinical Research Area Chief

  • Fernando Vazquez, MD · Internal Medicine Staff

  • Lourdes Posadas-MArtínez, MD · Internal Medicine Clinical research Area , HIBA

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-08-31
Primary Completion
2020-01-31
Completion
2020-01-31

Countries

  • Argentina

Study Locations

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Entities

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 NCT01372514 on ClinicalTrials.gov