Trials / Unknown
UnknownNCT01444508
Effect of Colloid Versus Crystalloid on Coagulation
Effect of Colloid Versus Crystalloid on Coagulation in Elective Urological Surgery
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 40 (estimated)
- Sponsor
- K. C. Rasmussen · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
In order to reduce bloodloss and need for transfusion to investigate the effect of colloid and crystalloid on coagulation assuming no difference between the groups.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ringer-lactate "SAD" | Lactated Ringer's is administrated intravenously in the dosis of max. 35 ml/kg during the operation after securing normovolaemia with Nexfin Monitor at induction of the anaesthesia: if bolus infusion of 200 ml increases stroke volume more than 10 % the patient is not assumed normovolaemic and bolus infusions are repeated until normovolaemic status is achieved. |
| DRUG | HES 130/04 | Voluven is administered intravenously in the doses of max. 35 ml/kg during the operation. Normovolaemia is achieved in the same way as described in intervention by Ringer-lactate "SAD". |
Timeline
- Start date
- 2011-09-01
- Primary completion
- 2013-04-01
- Completion
- 2013-12-01
- First posted
- 2011-09-30
- Last updated
- 2013-12-13
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT01444508. Inclusion in this directory is not an endorsement.