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
| Type | Name | Description |
|---|---|---|
| DRUG | venoferrum(iron sucrose) | administer once weekly calculated quantity of Venoferrum® ampoules according to body weight and Hb level. |
| DRUG | Bolgre (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.