Icarifil® in Association with Daily Use of Tadalafil (5 mg) versus Standard Tadalafil Daily Dose (5 mg) or Alone: Results from a Controlled, Randomized Clinical Trial

Author:

Cai Tommaso12ORCID,Palumbo Fabrizio3,Miacola Carlos4,Ceruti Carlo5,Rizzo Michele6,Liguori Giovanni6,Gallelli Luca7ORCID,Palmieri Alessandro8

Affiliation:

1. Department of Urology, Santa Chiara Regional Hospital, 38122 Trento, Italy

2. Institute of Clinical Medicine, University of Oslo, 0313 Oslo, Norway

3. Urology Unit, Di Venere Hospital, 70131 Bari, Italy

4. Department of Urology, University of Bari, 70121 Bari, Italy

5. Department of Urology, University of Turin, 10124 Turin, Italy

6. Department of Urology, University of Trieste, 34127 Trieste, Italy

7. Department of Health Science, School of Medicine, University of Catanzaro, 88100 Catanzaro, Italy

8. Department of Urology, University of Naples, Federico II, 80138 Naples, Italy

Abstract

Background: The management of erectile dysfunction (ED) shows several grey zones and new treatments are required to reduce the percentage of patients discontinuing treatment. Here, we aim to evaluate the role of a natural mixture named Icarifil® (L-Citrulline, L-Carnitine, Eruca vesicaria, Panax ginseng, Tribulus terrestris, Turnera diffusa, Taurine, Vitamin E, Zinc) in the management of patients with ED. Methods: From September 2022 to March 2023, all patients attending 3 urological institutions due to ED were randomized to receive the following for 3 months: Icarifil® 1 sachet every 24 h (Group 1) or Icarifil® 1 sachet + tadalafil 5 mg 1 tablet every 24 h (Group 2) or tadalafil 5 mg 1 tablet daily (Group 3). All patients underwent urologic visits and dedicated questionnaires (IIEF-5, SEP-2, SEP-3) at enrollment and at the follow-up evaluation (3 months). Patient-Reported Outcomes (PROs) at the follow-up evaluation were used. The primary endpoint was the difference in the questionnaires at the follow-up visit compared to the one at enrollment among the study groups. Results: In the per-protocol analysis, 52 patients in Group 1, 55 in Group 2 and 57 in Group 3 were analyzed. At the follow-up evaluation, IIEF-5 scores improved in all the 3 groups between enrollment and the follow-up evaluation, but a statistically significant difference was reported between Group 2 (+7.4) and Group 1 (+4.1) or Group 3 (+5.1), (p < 0.001; p < 0.001). Moreover, 47 patients (94.0%) in Group 2 showed an improvement in the SEP questionnaires, when compared with the baseline, while 29 in Group 1 (56.9%) and 42 in Group 3 (82.3%) showed a statistically significant difference (p = 0.004; p = 0.003) among the groups. The PRO analysis reported better efficacy and patient satisfaction in Group 2 when compared with Group 1 or Group 3. Conclusions: In conclusion, Icarifil® is able to improve penile erectile function in mild–moderate ED and significantly improve the clinical efficacy of daily used tadalafil 5 mg. Icarifil® could represent an interesting alternative treatment in patients experiencing adverse effects or with contraindications for chronic treatment with PDE5-is.

Publisher

MDPI AG

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5. (2024, February 03). Available online: https://www.marketdataforecast.com/market-reports/pde-inhibitors-market-revenue.

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