Back to Search Start Over

Oral Preparation of Hyaluronic Acid, Chondroitin Sulfate, Curcumin, and Quercetin (Ialuril ® Soft Gels) for the Prevention of LUTS after Intravesical Chemotherapy.

Authors :
Manfredi, Celeste
Spirito, Lorenzo
Calace, Francesco Paolo
Balsamo, Raffaele
Terribile, Marco
Stizzo, Marco
Romano, Lorenzo
Napolitano, Luigi
Califano, Gianluigi
Cirillo, Luigi
Fusco, Giovanni Maria
Rosati, Claudia
Quattrone, Carmelo
Sciorio, Carmine
Creta, Massimiliano
Longo, Nicola
De Sio, Marco
Arcaniolo, Davide
Source :
Pathophysiology; Sep2022, Vol. 29 Issue 3, p365-373, 9p
Publication Year :
2022

Abstract

Intravesical chemotherapy may cause chemical cystitis and related lower urinary tract symptoms (LUTS). The aims of this study were to evaluate the efficacy and safety of an oral preparation of hyaluronic acid (HA), chondroitin sulfate (CS), curcumin, and quercetin (Ialuril<superscript>®</superscript> Soft Gels) to reduce the severity of LUTS in patients with a history of bladder cancer (BCa) undergoing intravesical chemotherapy. We designed a monocentric, randomized, double-blind, placebo-controlled pilot trial. Patients referred to our institute between November 2016 and March 2018 were enrolled. All subjects had non-muscle-invasive BCa and received intravesical chemotherapy with mitomycin C (MMC). Patients were randomized 1:1 in two groups (intervention vs. control). All subjects underwent oral administration (Ialuril<superscript>®</superscript> Soft Gels or placebo) starting one week before the first weekly instillation and ending 30 days after the last one, subsequently starting one week before each monthly instillation and ending 14 days after it. International prostate symptom score (IPSS) and 0-100 visual analogue scale (VAS) were used to assess the efficacy of the treatment. Adverse events were also described. Patients were evaluated at baseline and after 1, 4, 7, and 13 months of intravesical chemotherapy. A total of 34 patients were enrolled. The median IPSS score was significantly lower in the intervention group compared to the control group at 4 (13 vs. 17 points; p = 0.038), 7 (10 vs. 18 points; p < 0.001), and 13 (10 vs. 17 points; p = 0.002) months. The median VAS score was significantly lower in the intervention group compared to the control group at 7 (22 vs. 37 points; p = 0.021) and 13 (20 vs. 35 points; p = 0.024) months. No AE specifically related to supplement or placebo was recorded. Oral formulation of HA, CS, quercetin, and curcumin could be an effective and safe supportive therapy against chemical cystitis in patients receiving intravesical chemotherapy for BCa. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09284680
Volume :
29
Issue :
3
Database :
Complementary Index
Journal :
Pathophysiology
Publication Type :
Academic Journal
Accession number :
171914450
Full Text :
https://doi.org/10.3390/pathophysiology29030028