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NCT00401908 Clinical Trial

Factors Contributing To Cardiovascular Morbidity and Mortality in Patients With Gastrointestinal Bleeding

Acute Coronary Syndrome Clinical Trial

Official title:
Factors Contributing To Cardiovascular Morbidity and Mortality in Patients With Gastrointestinal Bleeding

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00401908
Other study ID # 06-09-VA02
Secondary ID
Status Withdrawn
Phase N/A
First received November 17, 2006
Last updated September 25, 2015
Start date November 2006
Est. completion date October 2008

Study information
Verified date September 2015
Source Maimonides Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The rate of complication and death of patients with acute digestive tract bleeding is increased in the setting of acute coronary heart disease. The aim of the study is to establish the relative importance of the risk factors contributing to the death rate from acute digestive tract bleeding in patients admitted with acute coronary heart disease.

Description:

The rate of complication and death of patients with acute digestive tract bleeding is increased in the setting of acute coronary heart disease. The aim of the study is to establish the relative importance of the risk factors contributing to the death rate from acute digestive tract bleeding in patients admitted with acute coronary heart disease. This study will be conducted at MMC and involve collecting your clinical information from our medical records and computer systems. Approximately 200 adult patients with acute coronary heart disease and acute digestive tract bleeding admitted to MMC will be enrolled and followed up for 1 year after recruitment. We propose to develop criteria and a scoring system that will assist your doctors in caring for patients like you in the future.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date October 2008
Est. primary completion date October 2008
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Consecutive patients with acute CS and acute GI bleeding

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Maimonides Medical Center Brooklyn New York

Sponsors (1)
Lead Sponsor Collaborator
Maimonides Medical Center

Country where clinical trial is conducted

United States, 

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