Effect of Colloid Versus Crystalloid on Coagulation
- Registration Number
- NCT01444508
- Lead Sponsor
- K. C. Rasmussen
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 40
- Patient more than 18 years old
- Indication for elective post-renal operation including cystectomy
- Patient without anticoagulative, acetylsalicylic acid or NSAID treatment for the last 5 days.
- Intracerebral bleeding, manifest cardiac insufficient, renal insufficient demanding dialysis, hepatic or coagulation diseases
- Pregnant or nursing
- Allergic
- Disturbance in electrolytes
- Patient under committee
- Patient joining another trial interfering the actual trial.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description crystalloid Ringer-lactate "SAD" - colloid HES 130/04 -
- Primary Outcome Measures
Name Time Method Effect of colloid versus crystalloid on laboratory coagulation. 5-7 hours Coagulation is analysed in bloodsamples before, during (10 minutes post cystectomia), at the end of the operation and 2 hours later on.
The bloodsamples are analysed by thromboelastography (5000 series TEG analyzer, Haemoscope Corporation, Niles IL, USA) besides the classic coagulation parametres: platelet count, INR, Fibrinogen, APTT, D-dimer and Haemoglobin, Amylase and Creatinin.
- Secondary Outcome Measures
Name Time Method Effect of colloid versus crystalloid on the amount of bloodloss 5-7 hours The water balance inclusive the amount of bloodloss is registrated at the end of the operation and 2 hours later on.
Trial Locations
- Locations (1)
Rigshospitalet
🇩🇰Copenhagen, Denmark