Effectiveness of complete symptoms using Boenninghausens therapeutic pocket book in the Homoeopathic treatment of urinary tract infection in female- An open observational, prospective clinical study
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Visual analogue scale for pain assessment
研究概览
简要总结
Urinary tract infection is a common and painful clinical condition. The term UTI encompasses varities of clinical entities, including asymptomatic bacteriurea cystitis, prostatitis and pyelonephritis. UTI can be in any age group but most commonly occur in women in child bearing age group. Homoeopathy plays an important role in treating patient suffering from UTI. So an open observational, prospective clinical study to know the effectiveness of homoeopathic medicine in treatment of UTI will be taken in National Institute of Homoeopathy, Kolkata. Study has a target to achieve a sample of 40 patients. Outcome assesment will be done by using VAS scale for pain at base line and after 3 months. The score obtained by the patients will be compared and result will be analysed as per appropriate statistical methods and interference will be done thereafter.
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 18.00 Year(s) 至 50.00 Year(s)（—）
- 性别
- Female
入选标准
- •Patients with clinical findings of urinary tract infection and or pathological reports of urine routine/microscopic.
- •Female patients of age group 18-50 years.
- •Cases supported with urine routine/microscopic, culture report.
- •Patients willing to give written consent to participate in the study.
- •All the patients should know either of Hindi, English, or Bengali.
排除标准
- •Complicated cases of urinary tract infection.
- •Cases suffering from uncontrolled systemic illness or life-threatening illness.
- •Substance abuse and/or dependence.
- •Unwilling to take part and not giving consent to join the study.
- •Psychiatric patient.
- •Self-reported immune compromised state.
结局指标
主要结局
Visual analogue scale for pain assessment
时间窗: Baseline and after 3 months
次要结局
未报告次要终点