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[Yimusake Tablet: safe and efficacious for premature ejaculation].

Lian-ming Zhao1, Hui Jiang, Kai Hong

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Summary
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Yimusake Tablet significantly increased intravaginal ejaculation latency time (IELT) and patient satisfaction in men with premature ejaculation (PE). The treatment demonstrated a favorable safety profile with minimal adverse events, confirming its efficacy.

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Area of Science:

  • Clinical Urology
  • Pharmacological Research
  • Men's Health

Background:

  • Premature ejaculation (PE) is a common male sexual dysfunction impacting quality of life.
  • Objective evaluation of treatment efficacy and safety is crucial for PE management.
  • Yimusake Tablet is a potential therapeutic agent for PE.

Purpose of the Study:

  • To objectively evaluate the efficacy and safety of Yimusake Tablet for treating premature ejaculation (PE).
  • To assess the impact of Yimusake Tablet on intravaginal ejaculation latency time (IELT) and patient satisfaction.
  • To investigate the safety profile and adverse events associated with Yimusake Tablet treatment.

Main Methods:

  • A multi-centered, open-label, self-compared clinical trial involving 300 diagnosed PE patients.
  • 12-week trial duration: 4 weeks placebo, 8 weeks Yimusake Tablet (2 pills/night).
  • Primary outcome: change in IELT; secondary outcomes: patient satisfaction, safety, and erectile function (IIEF-5).

Main Results:

  • Mean IELT increased significantly from 62.5s at baseline to 222.2s after 8 weeks of Yimusake Tablet.
  • Patient satisfaction significantly improved; mild to moderate erectile dysfunction showed improvement in IIEF-5 scores.
  • Adverse events were mild (constipation, dry mouth, etc.) and resolved without treatment discontinuation.

Conclusions:

  • Yimusake Tablet is a safe and effective medication for treating premature ejaculation (PE).
  • The treatment offers significant improvements in ejaculatory latency and patient-reported outcomes.
  • The favorable safety profile supports its clinical utility in managing PE.