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NCT ID: NCT04148677 Not yet recruiting - Pain Clinical Trials

Protoves M1® Syrup in Controlling Adverse Event During HIVEC® Instillations

Start date: December 1, 2019
Phase:
Study type: Observational

100 patients with bladder cancer whose underwent Hyperthermic Intravesical Chemotherapy (HIVEC®) will be randomized in two groups (Group A: PROTOVES M1 SYRUP, Group B: NO TREATMENT). The aim of this study will be to analyse the role of two alkaloid, Protopine and Nuciferine (Protoves-M1 ®) in the prevention and the treatment of the low and mild grade adverse events related to the use of HIVEC® instillations.