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NCT00797589

Effect of Prime Solution on Fluid Balance After Open Heart Surgery

Completed Phase 4 Last updated 24 August 2015
What this trial tests

Phase 4 trial testing HES in Valve Surgery in 35 participants. Completed in 1 September 2012.

Timeline
1 January 2009
Primary endpoint
1 September 2012
1 September 2012

Quick facts

Lead sponsorUniversity of Helsinki
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment35
Start date1 January 2009
Primary completion1 September 2012
Estimated completion1 September 2012
Sites1 location across Finland

Drugs / interventions tested

Conditions studied

Sponsor

University of Helsinki

Who can join

18 and older, any sex, with Valve Surgery or Coronary Artery Bypass Grafting. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The use of Tetraspan® as prime solution can reduce fluid extravasation after perfusion versus Ringer acetate. Plasma-adapted HES-solutions produce also less acidosis.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Valve Surgery

Currently open trials in the same condition.

Other University of Helsinki trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00797589.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing