Trials / Completed
CompletedNCT02584868
Colloids in Pediatric Cardiac Surgery: Comparison Between a Balanced and a Non-balanced Colloid
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 88 (actual)
- Sponsor
- Queen Fabiola Children's University Hospital · Academic / Other
- Sex
- All
- Age
- 28 Days – 3 Years
- Healthy volunteers
- Not accepted
Summary
This study will compare the clinical efficacy and safety of Volulyte® and Voluven® during elective open-heart surgery in pediatric patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Hydroxyethyl starch 130/0.4 in an isotonic electrolyte solution | Peri-operative fluid replacement therapy (max 40ml/kg/day) |
| DRUG | Hydroxyethyl starch 130/0.4 in 0.9% sodium chloride | Peri-operative fluid replacement therapy (max 40ml/kg/day) |
Timeline
- Start date
- 2013-02-15
- Primary completion
- 2016-11-21
- Completion
- 2016-11-21
- First posted
- 2015-10-23
- Last updated
- 2020-11-09
- Results posted
- 2020-11-09
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT02584868. Inclusion in this directory is not an endorsement.