Factors Contributing To Cardiovascular Morbidity and Mortality in Patients With Gastrointestinal Bleeding
September 25, 2015 updated by: Ting-Hui Hsieh, Maimonides Medical Center
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.
Study Overview
Status
Withdrawn
Conditions
Detailed 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.
Study Type
Observational
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
Brooklyn, New York, United States, 11219
- Maimonides Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
General population.
Description
Inclusion Criteria:
- Consecutive patients with acute CS and acute GI bleeding
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Jianjun Li, MD, Maimonides Medical Center
- Principal Investigator: Scott M Tenner, MD, Maimonides Medical Center
- Principal Investigator: Jacob Shani, MD, Maimonides Medical Center
- Principal Investigator: Ting-Hui Hsieh, MD, Maimonides Medical Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2006
Primary Completion (Actual)
October 1, 2008
Study Completion (Actual)
October 1, 2008
Study Registration Dates
First Submitted
November 17, 2006
First Submitted That Met QC Criteria
November 20, 2006
First Posted (Estimate)
November 22, 2006
Study Record Updates
Last Update Posted (Estimate)
September 28, 2015
Last Update Submitted That Met QC Criteria
September 25, 2015
Last Verified
September 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 06-09-VA02
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.