Clinical Trials Directory

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

TypeNameDescription
DRUGRinger-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.
DRUGHES 130/04Voluven 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.