Clinical trial

Study to Evaluate the Effect of Hydroxyethyl Starch (HES) in Complications of…

NCT00308126 · Fresenius Kabi, Industry · Completed

Key facts

NCT number NCT00308126
Title Study to Evaluate the Effect of Hydroxyethyl Starch (HES) in Complications of Patients After Abdominal Surgery
Official title Phase IV, Open-Label, Randomized, Albumin-Controlled, Parallel Group, Multicenter Study to Evaluate the Effect of Medium Molecule HES (130/0.4) in Complications for Patients After Abdominal Surgery
Lead sponsor Fresenius Kabi, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Postoperative Complications
Intervention type Drug
Interventions Hydroxyethyl Starch 130/0.4 (Voluven)
Enrollment 624
Start date Jun 1, 2005
Completion Sep 1, 2006
First posted Mar 29, 2006
Last update posted Dec 11, 2007
Countries China

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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