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Beeinflussung Der Resorption Von Arzneimitteln Bei Stoma Patient*Innen
Peroral administration is the preferred way of taking medication. However, the special absorption conditions in ostomy patients are generally not addressed in approval studies and there is also little other literature on this topic. These are usually case reports or studies on individual patients or very small patient collectives. For medications with measurable clinical parameters, e.g. blood pressure, blood sugar, etc: Blood pressure, blood sugar, etc., these can be used to draw conclusions about any absorption problems. For medications without the possibility of a direct and objective assessment, the assessment is difficult due to the very low level of evidence. Drug groups without a direct physiological measure are e.g: Psy-chotropic drugs (antipsychotics, antidepressants, anxiolytics) and also the novel oral anticoagulants (NOACs). The clinical trial´s results will answer the following questions: * Are therapeutic blood levels of psychotropic drugs and NOACs achieved in ostomy patients when taken orally in the usual way? * Are there differences between the measured levels of ileostomy and colostomy patients? Colostomy and ileostomy patients undergoing inpatient or outpatient treatment at the Klinik Ottakring are ready for inclusion. The blood samples will be obtained during medically indicated and performed blood draws within the scope of medical practice, so that no study-associated risks arise here. Recorded and evaluated: * Relevant patient data * Plasma levels of the drugs under investigation in ostomy patients. The therapeutic range specified in the respective approval studies serves as the reference value. The results obtained are documented, evaluated and interpreted in an appropriate manner.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
WiGeV Klinik Ottakring
Vienna, Vienna, Austria
Start Date
June 18, 2025
Primary Completion Date
December 31, 2026
Completion Date
December 31, 2026
Last Updated
August 22, 2025
128
ESTIMATED participants
Monitoring
DIAGNOSTIC_TEST
Lead Sponsor
WiGeV Klinik Ottakring
NCT07338565
NCT06344078
Data Source & Attribution
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