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The aim of this study is to evaluate and optimize protocols for the isolation and analysis of analytes in urine (cell-free nucleic acids, extracellular vesicles and proteins). The following factors will be evaluated (1) volumetric collection with Colli-Pee®, a collection device developed by Novosanis for standardized collection of urine, and (2) stabilization methods. This is a prospective study in which urine samples will be collected from healthy volunteers, urine samples and a blood sample from pregnant women and cancer patients with solid tumors with emphasis on breast- and prostate cancer. The participants will be asked to provide a urine sample collected with the Colli-Pee® device and fill out an online questionnaire to collect usability data. Thereafter, the urine sample will be aliquoted to be used in different pilot studies for the protocol optimization. For the pilot study where the effect of volume will be assessed, participants will be requested to collect multiple samples with different Colli-Pee® variants and fill out questionnaires accordingly.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
Yes
Universitair ziekenhuis Antwerpen
Edegem, Antwerpen, Belgium
Start Date
June 18, 2020
Primary Completion Date
November 1, 2023
Completion Date
December 1, 2023
Last Updated
November 13, 2023
105
ACTUAL participants
Colli-Pee UAS devices
DEVICE
Lead Sponsor
Novosanis NV
Collaborators
NCT05673200
NCT05691465
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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