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OpenTrials
Completed

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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Key information

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

Restrictive VS Standard Fluid Regime

Procedure

Drag: Crystalloids and Colloids

Drug

Primary outcomes

  1. Number of major and minor complications

    Time frame: 30 days

Secondary outcomes

  1. ICU and duration of Hospital stay

    Time frame: 30 days

  2. In-hospital mortality, 30-days mortality

    Time frame: 30 days

  3. 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.