Clinical Trials Directory

Trials / Completed

CompletedNCT00802139

Efficacy and Safety Study of Iron Sucrose and Oral Iron Acetyl-transferrin Hydroglycerin

A Prospective, Randomized, Multi-centered Trial to Compare the Efficacy and Safety of Intravenous Iron Sucrose (Venoferrum®) With Oral Iron Acetyl-transferrin Hydroglycerin (Bolgre®) in Pregnant Women With Iron Deficiency Anemia

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
58 (actual)
Sponsor
JW Pharmaceutical · Industry
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

multi-center, prospective, randomized, open-labeled, active-drug-controlled, two-parallel-group-comparison(venoferrun group vs Bolgre group)study

Conditions

Interventions

TypeNameDescription
DRUGvenoferrum(iron sucrose)administer once weekly calculated quantity of Venoferrum® ampoules according to body weight and Hb level.
DRUGBolgre (Iron acetyl-transferase)Twice daily administration with Bolgre® soln (one pouch per dosing which is equivalent to 40mg of iron) for 5 weeks

Timeline

Start date
2008-02-01
Primary completion
2009-06-01
Completion
2010-10-01
First posted
2008-12-04
Last updated
2012-03-30

Locations

3 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT00802139. Inclusion in this directory is not an endorsement.