Status:
COMPLETED
Optimizing Iron Suppletion After Roux-en-Y Gastric Bypass
Lead Sponsor:
Rijnstate Hospital
Conditions:
Iron Deficiency
Eligibility:
FEMALE
18-65 years
Phase:
PHASE4
Brief Summary
Multicentre randomized controlled trial to evaluate the optimal treatment for patients who developed an iron deficiency after Roux-en-Y Gastric bypass.
Detailed Description
Morbid obesity is worldwide a still growing problem. The number of bariatric procedures are still increasing with 9000 bariatric operations in 2009. The golden standard is the Roux-en-Y Gastric bypass...
Eligibility Criteria
Inclusion
- all women who underwent a Roux-en-Y gastric bypass and developed an iron deficiency postoperatively (ferritin\<20microgram/L)
Exclusion
- iron deficiency peroperative, blood transfusions during study period, iron containing nutritional supplements except the standard multivitamins after bariatric surgery, decreased renal failure, excessive blood loss due to menstruation, anemia not caused by iron deficiency, accumulation of iron, hypersensitivity for noe of the medicinal products, psychiatric illness, pregnancy
Key Trial Info
Start Date :
December 4 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 6 2017
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT02271997
Start Date
December 4 2014
End Date
June 6 2017
Last Update
January 18 2019
Active Locations (3)
Enter a location and click search to find clinical trials sorted by distance.
1
OLVG West/ Sint Lucas Andreas Ziekenhuis
Amsterdam, North Holland, Netherlands, 1061 AE
2
Rijnstate hospital
Arnhem, Netherlands, 6800WC
3
Rose Kruis Ziekenhuis
Beverwijk, Netherlands