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Patients presenting for colonoscopy at one of the participating centers will be asked to participate in the present study after careful evaluation of inclusion and exclusion criteria. Before inclusion, all patients have to sign the written informed consent. All participating patients will receive PLENVU, a well-known and approved bowel preparation agent. Patients are randomly assigned in two groups. Patients in group 1 are informed in traditional way on how to use the bowel preparation agent. This way includes discussion with the physician and nurse on how to use the bowel preparation agent and a written documentation, highlighting the individual steps again. Patients in group 2 will receive in addition a QR-code referring to an App, available for free in all App stores, explaining to the patient in detail when and how to use the bowel preparation agent. The patient is receiving the same questionnaire (please see attached) in both groups and asked to bring the filled form on the day of the examination. Endoscopy is performed in standard way and effectiveness of the bowel preparation is specifically highlighted by the physician on the documentation report. Finally, data is analyzed regarding effectiveness of the QR code regarding patient satisfaction, acceptability and quality of the bowel preparation.
Full description
Patient education is of paramount importance for high acceptance and an adequate bowel preparation. Using the QR code directly referring to the App for bowel preparation with PLENVU might accelerate the discussion between the medical doctor and the patient and might also improve the acceptance rate of the patients for the bowel preparation finally leading to a more enhanced and effective bowel-preparation.
Patients undergoing screening or surveillance endoscopy will be prospectively included and randomly assigned to one of the following groups: Group 1: App; Group 2: no-App Study end points addressed below are prospectively assessed and evaluated for any significant changes.
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Inclusion criteria
• Screening or surveillance colonoscopy
Exclusion criteria
• Pregnancy or lactating
Lower gastrointestinal bleeding with hemodynamic instability
Bowel obstruction
ASA >3
Not sufficiently corrected anticoagulation disorders
Plenvu must not be taken:
Warnings and precautions
o You should tell your doctor about the following circumstances before taking Plenvu:
if you have heart problems and/or arrhythmias;
if you have kidney problems and/or suffer from dehydration;
if you have stomach or intestinal problems, including intestinal inflammation;
if you have difficulty or discomfort when swallowing liquids;
if you have high or low levels of electrolyte (e.g. sodium, potassium);
if you have other diseases (e.g. convulsions).
Pregnancy and lactation o There are no data on the use of Plenvu during pregnancy or lactation and is therefore not recommended.
404 participants in 2 patient groups
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Central trial contact
Tanja Bender, M.A.; Helmut Neumann, Prof. Dr.
Data sourced from clinicaltrials.gov
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