跳至主要内容
临床试验/CTRI/2024/03/064848
CTRI/2024/03/064848尚未招募Phase 3 4

A comparative study of Vilanterol/Fluticasone furoate with Formoterol/Budesonide in the management of stable bronchial asthma

SRM College of Pharmacy1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2024年4月10日最近更新:

试验速览

阶段
Phase 3 4
状态
尚未招募
发起方
入组人数
48
试验地点
1
主要终点
To assess the therapeutic effectiveness of Vilanterol/Fluticasone furoate with Formoterl/Budesonide by monitoring pulmonary function test (spirometry) FVC(L),%FVC,FEV1(L),%FEV1,FEV1/FVC,FEF25-75%

研究概览

简要总结

At present ,commonly used LABA ( long acting beta 2 agonist ) for asthma management require twice daily which is less convenient for patients and leads to reduced adherence with long term therapy whereas Vilanterol is a once daily therapy lead to improve adherence with long term therapy.Formoterol not highly selective in beta2 adrenoreceptor in lungs whereas vilanterol is highly selective for beta2 adrenoreceptor in lungs , in patients with asthma inhaled vilanterol produce significant increase in Forced Expiratory volume in 1s(FEV1). vilanterol /fluticasone furoate increase drug adherence to patients due to once daily administration. vilanterol/fluticasone cardioprotective

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
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • patients with stable bronchial asthma
  • patients who already receiving prescription with formoterol /budesonide.

排除标准

  • patients with asthma /copd overlap
  • patients with bronchiectasis
  • patients with allergic bronchopulmonary aspergillosis 4.history of smoking 5.pregnancy.

结局指标

主要结局

To assess the therapeutic effectiveness of Vilanterol/Fluticasone furoate with Formoterl/Budesonide by monitoring pulmonary function test (spirometry) FVC(L),%FVC,FEV1(L),%FEV1,FEV1/FVC,FEF25-75%

时间窗: In the initial ,patients FVC,%FVC ,FEV1,FEV1/FVC ,FEF25-75% will be evaluated ,mean changes in the parameters observed at 4th week,8th week ,12th week

次要结局

  • Quality of Life assessed by ACQ5 Questionnaire,ACT Scores & Adherence Barrier Survey(6 months)

研究者

发起方
SRM College of Pharmacy
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr .N .Nalini Jayanthi

SRM Medical college Hospital and Research Centre

研究点 (1)

Loading locations...

相似试验