About this trial

This research project examines the prevalence of medication-related dysphagia in patients with dysphagia-associated diseases. Its primary aim is to assess how frequently swallowing difficulties occur during medication intake and to evaluate the impact of different consistencies-such as semi-solid formulations and commercial swallowing gels-on the swallowing process. Flexible endoscopic evaluation of swallowing serves as the diagnostic gold standard to determine whether alternative administration forms can facilitate safer swallowing. The findings are intended to support the optimization of medication intake and the prevention of complications in patients with dysphagia.

Eligibility criteria

Qualifiers

None

Disqualifiers

None

Trial design

Treatments tested in this trial

  • medication swallowing

Treatment groups

500 Participants
are divided into 1 treatment group

Locations

3
University Hospital Düsseldorf40225, DüsseldorfNorth Rhine-Westphalia, Germany
University Hospital Münster48149, MünsterNorth Rhine-Westphalia, Germany
Hospital Osnabrücl Onsabrück Germany

Sponsors and collaborators

Heinrich-Heine University, Duesseldorf

Lead sponsor