Status:
COMPLETED
Iron Absorption Trial
Lead Sponsor:
Rijnstate Hospital
Conditions:
Iron Absorption
Bariatric Surgery
Eligibility:
All Genders
18-65 years
Phase:
PHASE4
Brief Summary
Introduction: There are indications that the absorption of oral iron supplementation is reduced after a Roux- en -Y gastric bypass. Nevertheless, oral preparations are used as standard therapy for iro...
Eligibility Criteria
Inclusion
- patients who are eligible for a primary Roux- en -Y gastric bypass and who have no pre-existing iron deficiency (serum ferritin between 20-200 micrograms/L)
Exclusion
- blood transfusion one month before ans in the study period. The use of iron containing nutritional supplements, except our standardized multivitamin supplements. Decreased function of the kidney with a GFR of \< 30ml/min and a serum creatinin below 50 micromol/L. Hb\< 7.4 mmol/L in females en Hb\< 8.4 mmol/L in males. Accumulation of iron. Hypersensitivity for ons of the medicinal products. Psychiatric illness. Pregnancy
Key Trial Info
Start Date :
August 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 4 2015
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT02228902
Start Date
August 1 2014
End Date
May 4 2015
Last Update
June 11 2020
Active Locations (1)
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1
Rijnstate hospital
Arnhem, Netherlands, 6800WC