Research and Clinical Value of New Classification for Premature Ejaculation:Multi-Center Research
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 568
- 试验地点
- 6
- 主要终点
- Change of score of Premature ejaculation diagnostic tool(PEDT)
研究概览
简要总结
An observational study on the effect of new classification for premature ejaculation.
详细描述
Premature ejaculation (PE) is one of the the most common male sexual dysfunctions and it has negative impacts on people's quality of life. According to the time that PE syndromes come out, PE is clinically divided to primary PE , which appear from the first sex ,and secondary PE ,which occurred after a period of normal ejaculation. This method of classification make little sense for treatment. In 2008, PE was divided into four types: primary PE, secondary PE, natural variable PE and premature-like ejaculatory dysfunction , and different types of premature ejaculation have their corresponding treatment. Both method of classification are based on the subjective feelings of patients, then whether certain objective test can be used to help diagnosing premature ejaculation? The drug treatment of PE mainly includes local anesthetics and selective 5- serotonin reuptake inhibitor (SSRI), and the selective penile dorsal nerve block is the most used surgery. But the efficacy of dapoxetine(a new SSRI for PE) and local anesthetics is only about 60-70% and 60%, respectively, while the efficacy of surgery is not exact without a standard surgical indication. We suppose that there may be different subtypes of the nerve of patients with premature ejaculation may exist in, which corresponds to a specific treatment.
In previous study, the investigators studied the somatic sensory pathway and autonomic nerve function of patients with premature ejaculation, and found that they were characterized by different neural electrophysiological characteristics. About 60% patients with primary PE show hypersensitivity of penis, and the efficacy of local anesthetics or selective penile dorsal nerve block for them reached 90%. While SSRI can reduce the excitability of the sympathetic nervous system in patients with PE, and the effect of this drug on patients with Sympathetic hyperexcitability is better than those without Sympathetic hyperexcitability. Thus doctors here have already been dividing patients who only suffer from PE(no other diseases mentioned in exclusion criteria)into 4 groups according to the results of nerve electrophysiological examination and give corresponding treatment: 1. Penile sensory hyperexcitability Group, using local anaesthetics(compound lidocaine cream)to treat; 2. Sympathetic hyperexcitability Group: using selective serotonin reuptake inhibitor(SSRI)(Dapoxetine) to treat. 3. Mixed type Group: both Penile sensory hyperexcitability and Sympathetic hyperexcitability: Combined use of two treatments above. 4. Other Group: result of nerve electrophysiological examination is normal: this group of patients will receive further examination to figure out the reason. This pattern of treatment has been used in clinical practice for years.
In this research, the investigators will systemically observe the result of this classification and treatment for 12 weeks. Patients will be asked for participating in this research. The questionnaires(IELT,PEDT,PEP) can be filled in when visited or online about every 4 weeks. If he refused , he would still receive the classified treatment but not enrolled in this research. After treatment of 12 weeks, the investigators will measure the change of IELT, PEDT, PEP, nerve electrophysiological examination and CGIC, then compare the efficacy of the treatment to that has been reported before. If anyone do not want to continue the treatment, he could quit from this research. Software SPSS17.0 will be used for data analysis. The age, height, weight, quantity table, the latency and amplitude of each group will be expressed by the mean add or subtract standard deviation. Quantitative data comparison among groups was analyzed by single factor variance analysis (one-way ANOVA and LSD), comparison of rate using x2 test, comparison of before and after treatment compared with paired t test. P<0.05 showed statistically significant difference.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 60 Years(Adult)
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Male aged between 18 and 60;
- •Men in stable heterosexual, monogamous relationships >6 months;
- •Symptom of PE: Ejaculation that always or nearly always occurs prior to or within 2 minute of vaginal penetration from the first sexual experience; the inability to delay ejaculation; and negative personal consequences, such as distress, bother, frustration, and/or the avoidance of sexual intimacy.
排除标准
- •Urinary system infection: Abnormal result of routine urine and prostatic fluid routine examination;
- •Abnormal sex hormone: Abnormal result of sex hormone examination;
- •Systemic disease: hypertension, diabetes mellitus, alcohol dependence syndrome, coronary heart disease, and Mental disorder;
- •Organic disorder: Abnormal palpation of external genitals, testis, epididymis and spermatic cord;
- •Drug influence: use of any drug for PE, e.g. SSRI , PDE-5, tramadol, etc;
- •Known drug allergy to amide-type local anaesthetics or dapoxetine;
- •Currently participating, or in the past 30 days quit a another clinical research independent with this research;
- •Drugs, alcohol or substance abuse in last 6 months;
- •moderate or more severe erectile Dysfunction.
结局指标
主要结局
Change of score of Premature ejaculation diagnostic tool(PEDT)
时间窗: After enrollment,after 12 weeks' treatment
A questionnaire to evaluate and diagnose premature ejaculation
The change of results of Nerve electrophysiological examination
时间窗: After enrollment,after 12 weeks' treatment
To measure the penile sensory excitability and penile skin sympathetic excitability.
Change of Intra-vaginal Ejaculation Latency Time(IELT)
时间窗: After enrollment,after 4 weeks' treatment,after 8 weeks' treatment,after 12 weeks' treatment
Most commonly used in research on premature ejaculation.
Change of grade Premature ejaculation profile(PEP)
时间窗: After enrollment,after 4 weeks' treatment,after 8 weeks' treatment,after 12 weeks' treatment
A questionnaire consists of 4 questions to evaluate the 4 aspects of the symptom of premature ejaculation
Clinical Global Impression of Change
时间窗: After 12 weeks' treatment
A single question to measure the change after treatment
Change of Chinese Index of Premature Ejaculation of five items(CIPE-5)
时间窗: After enrollment,after 12 weeks' treatment
A questionnaire to evaluate and diagnose premature ejaculation designed for Chinese people
次要结局
未报告次要终点
研究者
Baibing Yang
Resident of Nanjing Drum Tower Hospital
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
