Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07138326

Impact on the Absorption of Drugs in Ostomy Patients

Beeinflussung Der Resorption Von Arzneimitteln Bei Stoma Patient*Innen

Status
Recruiting
Phase
Study type
Observational
Enrollment
128 (estimated)
Sponsor
WiGeV Klinik Ottakring · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTMonitoringMonitoring

Timeline

Start date
2025-06-18
Primary completion
2026-12-31
Completion
2026-12-31
First posted
2025-08-22
Last updated
2025-08-22

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT07138326. Inclusion in this directory is not an endorsement.