RPCEC00000416已完成2 期
Efficacy and safety of the PROCTOKINASA® suppository in the treatment of acute pelvic inflammatory disease in Primary Care
Matanzas University of Medical Sciences0 个研究点目标入组 76 人开始时间: 2023年2月9日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 76
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled trial. Masking: Open. Control group: Active. Assignment: Parallel. Purpose: Treatment
入排标准
- 年龄范围
- 19 years 至 one（—）
- 性别
- Female
入选标准
- •1. Female patients with a clinical and ultrasound diagnosis of mild and moderate acute pelvic inflammatory disease who have signed the informed consent.
- •2. Patients over 18 years of age.
- •3. Patients who do not require hospitalization.
排除标准
- •1. Patients who are participating in another clinical trial.
- •2. Breastfeeding patients.
- •3. Patients with a history of hypersensitivity to the product or to any of the components of the formulation.
- •4. Female patients with a clinical and ultrasound diagnosis of severe PID or with criteria for hospitalization.
- •5. Patients with surgery for less than 7 days, active bleeding or previously diagnosed bleeding disorder.
- •6. Patients with a diagnosis of arterial hypertension.
研究者
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