非溶剂型花粉提取物对健康女性尿失禁患者的疗效:随机、双盲、安慰剂对照、平行研究

Marc Moulin, Erin D Lewis, David C. Crowley, Colleen E. May, Malkanthi Evans
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引用次数: 0

摘要

尿失禁(UI)是一种使人衰弱的常见疾病,会对生活质量产生不利影响。治疗尿失禁症状的处方和手术方法可能会带来不良风险和并发症。这项随机、双盲、安慰剂对照、平行研究调查了两种非溶剂花粉提取物对健康女性尿失禁的疗效。 114名年龄在40-75岁之间、尿失禁国际咨询问卷-尿失禁简表(ICIQ-SF)得分≥5分的女性被随机分配到Graminex® RCT Fem™ UI、Graminex® PollenBerry®或安慰剂中,接受为期24周的治疗。主要结果是补充 24 周后试验组和安慰剂组之间 ICIQ-SF 分数的变化。次要结果包括补充 6、12、18 和 24 周后夜尿频率(记录在 3 天排尿日记中)和 24 小时漏尿量(通过尿垫重量评估)的变化,以及补充 24 周后压力引起的漏尿量(完成刺激性动作挑战后)的变化。 所有组别在第 24 周时的 ICIQ-SF 评分均有所改善(p < 0.001)。RCT Fem™ UI 组的 ICIQ-SF 评分改善幅度最大(-4.07 ± 3.4),其次是 PollenBerry® 组(-3.34 ± 2.87)和安慰剂组(-2.61 ± 3.52)。RCT Fem™ UI 组的 24 小时漏尿量(-17.68 ± 39.84 克)和夜尿次数(-0.52 ± 1.26)均有相应改善(p ≤ 0.05)。第24周时,补充 PollenBerry® 能明显改善压力引起的漏尿量(-7.12 ± 15.64 g)。研究产品的血液学和化学成分均符合安全标准。 服用 RCT Fem™ UI 补充剂后,尿频尿急的严重程度明显降低,每日漏尿量和夜尿次数也得到相应改善,具有临床意义。PollenBerry® 能明显改善压力引起的漏尿量,这表明它可能对容易出现压力性尿失禁的女性有效。该研究产品在此类人群中安全且耐受性良好。
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Efficacy of nonsolvent flower pollen extracts in healthy women with urinary incontinence: A randomized, double-blind, placebo-controlled, parallel study
Urinary incontinence (UI) is a debilitating and common condition that adversely affects quality of life. Prescriptive and surgical approaches for managing UI symptoms may result in undesirable risks and complications. This randomized, double-blind, placebo-controlled, parallel study investigated the efficacy of 2 nonsolvent flower pollen extracts on UI in healthy women. One-hundred and fourteen women aged 40–75 years who scored ≥5 on the International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-SF) were randomized to receive either Graminex® RCT Fem™ UI, Graminex® PollenBerry®, or placebo for 24 weeks. The primary outcome was the change in the ICIQ-SF score between the trial and placebo groups after 24 weeks of supplementation. The secondary outcomes included changes in the frequency of nocturia (recorded in 3-day void diaries) and 24-hour leakage volume (assessed via pad weight) after 6, 12, 18, and 24 weeks of supplementation and changes in stress-induced urinary leakage volume (after completion of a provocative maneuver challenge) after 24 weeks of supplementation. All the groups demonstrated improvement in ICIQ-SF scores at week 24 (p < 0.001). The RCT Fem™ UI group had the greatest improvement in ICIQ-SF scores (−4.07 ± 3.4), followed by the PollenBerry® group (−3.34 ± 2.87) and placebo group (−2.61 ± 3.52). The RCT Fem™ UI group had corresponding improvements in 24-hour leakage volume (−17.68 ± 39.84 g) and frequency of nocturia (−0.52 ± 1.26) (p ≤ 0.05). PollenBerry® supplementation significantly improved stress-induced urinary leakage volume (−7.12 ± 15.64 g) at week 24. The study products demonstrated safe hematological and chemical profiles. RCT Fem™ UI supplementation resulted in significant and clinically meaningful reductions in UI severity, with corresponding improvements in daily urinary leakage volume and frequency of nocturia. PollenBerry® significantly improved stress-induced urinary leakage volume, suggesting that it may be efficacious in women who are prone to stress UI. The study products were safe and well tolerated in this population.
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