Adult Cardiac Surgery Clinical Trial
NCT number | NCT02407574 |
Other study ID # | FFR2015 |
Secondary ID | |
Status | Not yet recruiting |
Phase | N/A |
First received | March 24, 2015 |
Last updated | March 30, 2015 |
Start date | May 2015 |
Verified date | March 2015 |
Source | University Hospital of Liege |
Contact | n/a |
Is FDA regulated | No |
Health authority | Belgium: Ethics Committee |
Study type | Interventional |
The aim of the study is to determine whether increasing the heart rate by epicardial atrial pacing after surgery improves the contractile force of the myocardium. After complete weaning from CPB, several pressure-loops of the LV will be recorded at different levels of preload using transoesophageal echo, invasive blood pressure monitoring. The preload will be manipulated by adding fluid from the CPB reservoir or draining fluid into the CPB reservoir.
Status | Not yet recruiting |
Enrollment | 20 |
Est. completion date | |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - CABG only surgery - Preopeartive LVEF = 53 % - Use of epicardial pacing wires to assist CPB weaning Exclusion Criteria: - Contra-indication to TEE - AV block at the time of CPB weaning - Sinus rhythm less than 50 or more than 90 BPM after CPB weaning. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University Hospital of Liege |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | End-systolic elastane of the left ventricle. | 30 minutes after CPB weaning | No |
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