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临床试验/TCTR20240816005
TCTR20240816005招募中3 期

Clinical Study on the Efficacy of 2% Povidone-Iodine Solution for Urethral Irrigation in the Treatment of Male Gonorrhea

The First Affiliated Hospital of Gannan Medical University0 个研究点目标入组 48 人开始时间: 2024年8月16日最近更新:

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
48

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
15 Years 至 60 Years(—)
性别
Male

入选标准

  • Adult male patients diagnosed with gonorrhea through NAATs and confirmed by urethral discharge microscopy.
  • Age between 18 and 60 years.
  • Ability to provide informed consent.
  • No known allergies to iodine or povidone-iodine.
  • No concomitant sexually transmitted infections other than gonorrhea.

排除标准

  • Patients aged over 60 years.
  • Patients with a history of allergic reactions to iodine or povidone-iodine.
  • Concomitant infections with Chlamydia, Mycoplasma, or other sexually transmitted infections.
  • Presence of urinary tract anomalies such as urethral strictures or hypospadias.
  • History of antibiotic treatment for gonorrhea within the last 4 weeks.

研究者

发起方
The First Affiliated Hospital of Gannan Medical University

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