Trials / Terminated
TerminatedNCT01303250
Perioperative Colloid vs Crystalloid in Patients Undergoing Colorectal Surgery
Balanced 6 % HES 130/0.4 vs. Balanced Crystalloid-based Infusion in Patients Undergoing Colorectal Surgery
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 31 (actual)
- Sponsor
- University Hospital Muenster · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The primary purpose of this study is to determine the effect of a balanced 6%hydroxyethyl starch 130/0.4 vs. a balanced crystalloid in colorectal surgery. The intraoperative fluid management will be given to optimize the stroke volume variation \<= 12%. The investigators hypothesize that patients in the intervention group will need less fluid administration be optimal hemodynamic stabilized.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | balanced 6% hydroxyethylstarch 130/0.4 | Fluid administration and optimization based on cardiac output findings during surgery. |
| DRUG | balanced crystalloid | Fluid administration and optimization based on cardiac output findings during surgery. |
Timeline
- Start date
- 2011-04-01
- Primary completion
- 2015-04-01
- Completion
- 2015-04-01
- First posted
- 2011-02-24
- Last updated
- 2015-12-18
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT01303250. Inclusion in this directory is not an endorsement.