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Clinical Trial Summary

To analyze the clinical impact of a food supplement composed of D Mannose, cranberry extract (Cran-max) and Vitamin D3 in the prevention of recurrent lower urinary tract infections (UTI)


Clinical Trial Description

Once patients have been informed about the study, the potential risks and treatment alternatives, those who meet the selection criteria, agree to participate and sign the informed consent, will be randomly and openly assigned, in a 1:1:1 ratio, to one of the following groups: Group A: Patients with repeat UTIs who will receive prophylactic treatment for 6 Months. Group B: Patients with repeat UTIs who will receive prophylactic treatment for 3 Months. Control group: Patients with recurrent UTIs who will not receive as prophylactic treatment the supplement under study. The three groups will be treated following standard clinical practice with follow-up at 3, 6, 9 and 12 months after inclusion. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04880343
Study type Interventional
Source Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz
Contact
Status Suspended
Phase N/A
Start date January 26, 2021
Completion date January 26, 2024

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