Does Modified Ultrafiltration Improves Inflammatory Response and Cardiopulmonary Function After CABG Procedures?
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| ClinicalTrials.gov Identifier: NCT01140113 |
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Recruitment Status :
Completed
First Posted : June 9, 2010
Last Update Posted : July 23, 2013
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Coronary Artery Disease Cardiac Surgical Procedures | Procedure: Modified Ultrafiltration | Not Applicable |
Show detailed description
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 60 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Double (Participant, Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | Does Modified Ultrafiltration Improves Inflammatory Response and Cardiopulmonary Function After CABG Procedures? |
| Study Start Date : | July 2007 |
| Actual Primary Completion Date : | July 2008 |
| Actual Study Completion Date : | March 2009 |
| Arm | Intervention/treatment |
|---|---|
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No Intervention: Placebo
this group had undergone to routine coronary artery bypass graft surgery
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Experimental: Modified Ultrafiltration
patients after weaning from bypass were submitted to ultrafiltration
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Procedure: Modified Ultrafiltration
After weaning from bypass patients had undergone to modified ultrafiltration for 15 minutes with a filtration flow at 300 ml/min
Other Name: Ultrafiltration |
- Overall clinical improvement after cardiac surgeries. [ Time Frame: 30 day after surgery ]
- The treatment group has less inflammatory markers [ Time Frame: 30 days ]
- The treatment group has improvements in the respiratory variables [ Time Frame: 30 ]
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| Ages Eligible for Study: | 30 Years to 90 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- elective patients to coronary artery bypass graft surgery
- left ventricle ejection fraction higher than 40%
Exclusion Criteria:
- renal impairment (serum creatinine higher than 1.7 mg%)
- neoplasm
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01140113
| Brazil | |
| Hospital da Clinicas | |
| Campinas, Sao Paulo, Brazil, 13100000 | |
| Principal Investigator: | Orlando Petrucci, MD, PhD | University of Campinas |
| Responsible Party: | Orlando Petrucci, MD, PhD, University of Campinas, Brazil |
| ClinicalTrials.gov Identifier: | NCT01140113 |
| Other Study ID Numbers: |
Modified Ultrafiltration |
| First Posted: | June 9, 2010 Key Record Dates |
| Last Update Posted: | July 23, 2013 |
| Last Verified: | July 2013 |
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hemoconcentration ultrafiltration coronary artery disease |
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Coronary Artery Disease Myocardial Ischemia Coronary Disease Heart Diseases |
Cardiovascular Diseases Arteriosclerosis Arterial Occlusive Diseases Vascular Diseases |

