Levothyroxine Sodium in Thyroidectomized Patients Taking Proton Pump Inhibitors

Exclusion Criteria

• •1. suspected or ascertained non-compliance with LT4 or PPI therapy;
• •2. subject requiring changes of levothyroxine dose;
• •3. use of over-the-counter (OTC) PPIs;
• •4. history of malabsorption or history of gastric bypass surgery, short-gut syndrome, inflammatory bowel disease and other conditions of the gastrointestinal tract that may affect drug absorption (e.g. celiac disease)3;
• •5. multiple co-morbidities (e.g. cardiac heart failure, active arrhythmia or history of arrhythmia, particularly atrial fibrillation, uncompensated diabetes mellitus, uncorrected adrenal insufficiency, seriously compromised hepatic, renal and/or respiratory functions);
• •6. neoplastic pathology, active or in remission for less than 5 years (excluding the basic thyroid pathology);
• •7. terminal condition;
• •8. parenteral or assisted enteral feeding;
• •9. presence of any medical condition or other circumstances which would significantly affect the safety of the subject or decrease the chance of obtaining reliable data, achieving study objectives or completing the study;
• •10. history of alcoholism, drug abuse or psychiatric diseases that could invalidate the informed consent or limit the subject compliance with protocol requirements;
• •11. pregnant (positive urine pregnancy test at screening or baseline visits) or breast-feeding subject or subject planning a pregnancy in the next months;
• •12. known hypersensitivity to the ingredients of the preparation involved in the study3;
• •13. use of forbidden concomitant medications;
• •14. regular consumption of soy and soy derivatives, cotton seed meals, walnuts, and dietary fibres;
• •15. participation in other clinical studies during the 3 months prior to screening;
• •16. presumption of poor reliability/cooperation;
• •17. any reason which, in the opinion of the Investigator, would prevent the subject from participating in the study.