ITMCTR2200005505尚未招募未知
Obstetrics and Gynecology
Obstetrics & Gynecology Hospital of Fudan University0 个研究点开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional study
入排标准
- 年龄范围
- 20 至 60（—）
- 性别
- Female
入选标准
- •1. Cervical cancer stage Ib1-IIa2 (2009 FIGO cervical cancer clinical staging) patients of 20-60 years old who have urinary retention after the catheter is removed 14-60 days after radical hysterectomy, whose residual urine is more than 100ml measured for two consecutive days.
- •2. The operation record confirmed that the operation method was radical hysterectomy;
- •3. Patients whoes expected survival time is more than 12 months;
- •4. Patients who agree to participate in this trial and have signed an informed consent form.
排除标准
- •1. Patients who have received pelvic radiotherapy in the past;
- •2. Patients older than 60 years old or younger than 20 years old;
- •3. Patients who undergo radical hysterectomy which have not been confirmed by surgery and pathology;
- •4. Patients with previous symptoms such as urinary dysfunction, urinary incontinence, or abnormal preoperative urodynamic tests;
- •5. Patients with severe urinary tract infection or vesicovaginal fistula;
- •6. Patients who are in the acute stage of other diseases: impaired consciousness, body temperature greater than 38°C, unstable vital signs or acute abdomen, etc.;
- •7. Patients who have important organ function impairment: liver enzymes> 2 times the upper limit of normal, creatinine> 2 times the upper limit of normal, blood amylase> 2 times the upper limit of normal, heart function grade 3-4, etc.;
- •8. Patients who have brain disease or abnormal judgment ability;
- •9. Patients who have drug and/or alcohol abuse;
- •10. Patients with mental illness receiving medication;
- •11. Patients who participated in other clinical trials within 4 weeks before the start of this study.
研究者
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