NCT Number: NCT01939652
Restrictive Versus Standard Fluid Regime in Elective Minilaparotomy Abdominal Aortic Aneurysm Repair
Elective minilaparatomy abdominal aortic aneurysm (AAA) repair is associated with a significant number of complications involving respiratory, cardiovascular, gastrointestinal and central nervous system, and mortality ranging up to 5%. In our study, we tested the hypothesis that intraoperative and postoperative intravenous restrictive fluid regime reduces postoperative morbidity and mortality and improves the outcome of the treatment of minilaparotomy AAA repair.
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Notify MeKey information
Sex eligibility
All sexes
Study type
Interventional
Phase
Early Phase 1
About this study
We investigate effects of a restricted fluid regime versus standard regimen on complications and hospital stay after minilaparatomy aortic aneurysm repair.
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- AAA more than 5,5 cm in diameter tube graft
Exclusion criteria
- emargency comorbidity maligancy
Treatment and study plan
Drag: Crystalloids and Colloids
DrugPrimary outcomes
-
Number of major and minor complications
Time frame: 30 days
Secondary outcomes
-
ICU and duration of Hospital stay
Time frame: 30 days
-
In-hospital mortality, 30-days mortality
Time frame: 30 days
-
Fluid balance (daily and cumulative)
Time frame: 3 days
Sponsors and collaborators
Lead sponsor
University Clinical Center Tuzla
Other
Registry information
Important dates
- Study start
- 2009
- Primary completion
- 2013
- Study completion
- 2013
- First posted
- Sep 11, 2013
- Registry last updated
- Sep 11, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.