2018
DOI: 10.5152/tud.2018.50328
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Comparison of safety and efficacy of silodosin, solifenacin, tadalafil and their combinations in the treatment of double-J stent- related lower urinary system symptoms: A prospective randomized trial

Abstract: Combination therapy with silodosin and solifenacin (group E) was effective for relieving SRS with improved quality of life and less requirement of analgesic than any other groups and should be considered in patients who develop SRS.

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Cited by 22 publications
(38 citation statements)
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“…We further excluded 41 articles due to lack of the use of the USSQ or USSQ completion at several time points, no use of placebo or considerable lack of data. Overall, eight papers, published between 2006 and 2018 were eligible for the meta-analysis, including 1350 patients receiving tamsulosin 0.4 mg, alfuzosin 10 mg or placebo and were compared with silodosin 8 mg, solifenacin 5 mg, tadalafil 5 mg, or combinations [8][9][10][11][12][13][14][15]. The aforementioned stages are illustrated in detail in Figure 1 and all studies are listed in Table 1 [8][9][10][11][12][13][14][15].…”
Section: Resultsmentioning
confidence: 99%
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“…We further excluded 41 articles due to lack of the use of the USSQ or USSQ completion at several time points, no use of placebo or considerable lack of data. Overall, eight papers, published between 2006 and 2018 were eligible for the meta-analysis, including 1350 patients receiving tamsulosin 0.4 mg, alfuzosin 10 mg or placebo and were compared with silodosin 8 mg, solifenacin 5 mg, tadalafil 5 mg, or combinations [8][9][10][11][12][13][14][15]. The aforementioned stages are illustrated in detail in Figure 1 and all studies are listed in Table 1 [8][9][10][11][12][13][14][15].…”
Section: Resultsmentioning
confidence: 99%
“…The duration of treatment with α-blockers varied between 1 and 8 weeks. Multi-length JJ stents composed of polyurethane [8,[11][12][13][14], silicone [15] and proprietary co-polymer [9,10] were used.…”
Section: Resultsmentioning
confidence: 99%
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“…Only three studies fulfilled the methodological requirements, i.e., the population base of 280 patients is quite limited. The three randomized control trials collected for analysis in this study are with significant heterogeneity in study design, especially in comparison with different drugs (Aggarwal et al [2]: tadalafil 5 mg vs placebo vs tamsulosin 0.4 mg; Bhattar et al [3]: tadalafil 5 mg vs placebo vs silodosin 8 mg; Tharwat et al [4]: sildenafil 50 mg vs placebo), which made the data less comparable. 2.…”
mentioning
confidence: 99%