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临床试验/CTRI/2025/01/079116
CTRI/2025/01/079116
尚未招募
不适用

Comparison of Silodosin Monotherapy vs FDC of Silodosin with Tadalafil in the Management of LUTS associated with BPH : An Open-Label Randomized Controlled Trial

Harshavardhan K1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年1月31日最近更新:

概览

阶段
不适用
状态
尚未招募
发起方
Harshavardhan K
入组人数
60
试验地点
1
主要终点
1.The study is to measure the change in IPSS from baseline to 12 weeks.

概览

简要总结

Primary Objectives

To evaluate the severity of LUTS and monitor symptom improvement using International Prostate Symptom Score  scale.

To assess changes in urinary flow rate is measured by using uroflowmetry

Secondary Objectives

To assess improvement in quality of life using the international Consultation on Incontinence Questionnaire Male Lower Urinary Tract Symptoms (ICIQ-MLUTS) scale.

To compare the onset and duration of symptom relief between the two groups.

To evaluate the safety, efficacy and tolerability of the FDC compared to silodosin alone.

To assess changes in post-void residual urine volume and prostate size is measured by Ultrasound.

Background & Justification for the conduct of the study

Benning Prostatic hyperplasia is a common condition cause predominantly on the elderly people over the age of 50. BPH mostly leads to LUTS . It significantly affects the quality of life of the men. Incomplete bladder emptying, nocturia, urgency, increased urine frequency, and weak urine stream are the most common symptoms. BPH leads to LUTS due the compression of the enlarged prostate compressing the bladder and the increased smooth muscle tone in the prostate and bladder neck. Medication remains the first-line treatment for patients with moderate to severe symptoms. Mostly Alpha-1 blockers are mostly used as it works by relaxing the prostate muscle thus alleviate symptoms. PDE-5 inhibitors are primarily used to treat erectile dysfunction but it shows beneficial action on LUTS in BPH patients by relaxing both prostate muscle and bladder neck. Several studies suggested that combination of this both may produce superior

relief to BPH patients. Still it needs well-designed clinical trials to confirm this findings to establish its efficacy and safety. Even with effective available treatment option but still get sonly the suboptimal relief of symptoms. Using the International Prostate Symptom Score IPSS, Uroflowmetry, Ultrasound the symptom improvement can be evaluated. Further this study may help in assessing the safety and tolerability of the combination therapy which may later can be applied in clinical practice.

Study Hypothesis

The combination of silodosin and Tadalafil may provide superior symptomatic relief in LUTS by measuring IPSS and Uroflowmetry parameters compared to silodosin alone by without any greater Adverse events.

Methodology:

Study design:

Open label, Randomized Controlled Trail.

Blinding:

Open label

Sample size

120 participants

60 participants with Silodosin 8mg Monotherapy group.

60 participants with FDC Silodosin 8mg with Tadalafil 5mg group.

Number of groups:

2 groups

Control group1: Silodosin 8mg monotherapy

Test group 2: Fixed-dose combination of Silodosin 8mg with Tadalafil 5mg.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
50.00 Year(s) 至 80.00 Year(s)(—)
性别
Male

入选标准

  • Aged above 50 years
  • Participants must have a clinical diagnosis of BPH with at least moderate LUTS, indicated by an International Prostate Symptom Score (IPSS) of 8 or higher, and a peak urinary flow rate (Q max) of 15 ml/sec or less
  • A post-void residual (PVR) volume of up to 200 ml
  • Provided inform consent and agreed to follow study protocols.

排除标准

  • Participants with any history of prostate cancer or recent prostate surgeries
  • Severe hepatic or renal impairment
  • Cardiovascular conditions such as recent myocardial infarction, stroke, or uncontrolled blood pressure, severe arrythmia, hypotension or orthostatic hypotension
  • Urological conditions like neurogenic bladder, bladder stones, or recurrent urinary tract infections
  • Hypersensitivity to either silodosin or tadalafil
  • substance abuse
  • Presence of Non- arteritic anterior ischemic optic neuropathy
  • Retinitis pigmentosa
  • Concurrent use of nitrates or nitroprusside.

结局指标

主要结局

1.The study is to measure the change in IPSS from baseline to 12 weeks.

时间窗: Visit 1- On Day 1, Baseline | Visit 2- 2nd week | Visit 3- 6th week | Visit 4- 12th week

2.To provide rapid and optimal relief from the symptoms.

时间窗: Visit 1- On Day 1, Baseline | Visit 2- 2nd week | Visit 3- 6th week | Visit 4- 12th week

3.To reduce the prostatic smooth muscle size.

时间窗: Visit 1- On Day 1, Baseline | Visit 2- 2nd week | Visit 3- 6th week | Visit 4- 12th week

次要结局

  • 1.Evaluate improvements in quality of life related to urinary symptoms.(2.Assess post-void residual volume to evaluate bladder emptying efficiency.)

研究者

发起方
Harshavardhan K
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Harshavardhan K

SRM medical college hospital and research centre.

研究点 (1)

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