Clinical Trials Directory

Trials / Terminated

TerminatedNCT00936247

Tetraspan 6 Percent (%) Combined With Sterofundin ISO Versus Albumin 5 Percent (%) Combined With Sodium Chloride (NaCL)

Prospective, Controlled, Single-blind, Bicentric, Randomized Study on the Safety of HES 130/0.42 Combined With a Bal. Electr. Sol. vs 5% Albumin Comb. With an Unbal. Electr. Sol. (NaCl 0.9%) in Pat. With Compensated Renal Failure

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
2 (actual)
Sponsor
B. Braun Melsungen AG · Industry
Sex
All
Age
50 Years – 80 Years
Healthy volunteers
Not accepted

Summary

This investigational study will investigate two different volume replacement regimes in patients suffering from compromised renal function.

Conditions

Interventions

TypeNameDescription
DRUGHES 130/0.42 + electrolyte solutionTetraspan 6% as colloid component combined with Sterofundin ISO as electrolyte component
DRUGAlbumin + electrolyte solutionAlbumin 5% as colloid component and NaCl 0.9% as electrolyte component

Timeline

Start date
2009-11-01
Primary completion
2010-09-01
Completion
2010-09-01
First posted
2009-07-09
Last updated
2010-09-28

Locations

2 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT00936247. Inclusion in this directory is not an endorsement.