Impact of Preoperative Martial Deficiency on the Level of Blood Transfusion in Programmed Cardiac Surgery
CARMATS
1 other identifier
observational
444
1 country
2
Brief Summary
Observational study.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2016
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 14, 2016
CompletedFirst Submitted
Initial submission to the registry
August 23, 2017
CompletedFirst Posted
Study publicly available on registry
August 25, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 15, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
January 15, 2018
CompletedSeptember 18, 2018
September 1, 2018
1.2 years
August 23, 2017
September 17, 2018
Conditions
Outcome Measures
Primary Outcomes (1)
Incidence of patients with iron deficiency
Baseline
Study Arms (1)
Thoracic Surgery
Observational study. It is only a matter of collecting clinical data.
Interventions
Observational study. It is only a matter of collecting clinical data.
Eligibility Criteria
All adult patients programmed for cardiac surgery
You may qualify if:
- All adult patients programmed for cardiac surgery in the cardiothoracic surgery departments of Rennes, Poitiers, and Brest.
You may not qualify if:
- Children \<18 years;
- Procedures for endovascular surgery;
- Vascular surgery other than ascending aorta and lacrosse;
- Non-cardiac thoracic surgery;
- Persons of full age who are subject to legal protection (safeguard of justice, curatorship, guardianship), persons deprived of their liberty.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Brest University Hospital
Brest, 29609, France
Rennes University Hospital
Rennes, 35033, France
Study Officials
- PRINCIPAL INVESTIGATOR
Baptiste Gaudriot
CHU Rennes
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 23, 2017
First Posted
August 25, 2017
Study Start
November 14, 2016
Primary Completion
January 15, 2018
Study Completion
January 15, 2018
Last Updated
September 18, 2018
Record last verified: 2018-09