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Iron Supplementation for Acute Anemia After Postbariatric Abdominoplasty — ISAPA  

Weight Loss Clinical Trial

Official title:
Iron Supplementation for Acute Anemia After Postbariatric Abdominoplasty: a Randomized Controlled Trial

Clinical Trial Summary

The purpose of this study is to determine whether intravenous or oral iron are effective in the treatment of postoperative anemia and iron deficiency in patients submitted in postbariatric abdominoplasty.

Clinical Trial Description

Multicenter open randomized clinical trial with allocation ratio 1: 1. 56 adult patients undergoing post- bariatric abdominoplasty will be evaluated. The study group will receive 200 mg of intravenous iron in the immediate postoperative period and a second application on day 1 postoperatively. The control group will receive 100 mg of oral iron twice daily for 8 weeks. Haematological variables , iron 's profile , quality of life ( SF -36 and FACT- An) and adverse events will be assessed preoperatively and on the first , fourth and eighth weeks postoperatively . ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01857011
Study type Interventional
Source Federal University of São Paulo
Contact
Status Completed
Phase Phase 3
Start date April 2014
Completion date June 2016
View Details
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