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临床试验/NCT01982968
NCT01982968已完成不适用

Weighing Risks and Benefits of Laparoscopic Anti-Reflux Surgery in Patients With Idiopathic Pulmonary Fibrosis

University of California, San Francisco5 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2013年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
58
试验地点
5
主要终点
Forced Vital Capacity (FVC)

研究概览

简要总结

This study will test the hypothesis that treatment with laparoscopic anti-reflux surgery in subjects with idiopathic pulmonary fibrosis (IPF) and abnormal gastroesophageal reflux (GER) will slow the decline of forced vital capacity (FVC) over 48 weeks.

详细描述

This protocol proposes to test the following hypothesis: Treatment with laparoscopic anti-reflux surgery in subjects with idiopathic pulmonary fibrosis (IPF) and abnormal gastroesophageal (GER) reflux will slow the decline of forced vital capacity (FVC) over 48 weeks. This study will randomize approximately 58 subjects with IPF and abnormal acid reflux on 24-hour impedance / pH monitoring to laparoscopic anti-reflux surgery or standard care (randomization ratio 1:1). Subjects will be followed for 48 weeks or until the time of lung transplantation or death.

We aim to achieve the following: determine the impact of laparoscopic anti-reflux surgery on change in FVC over 48 weeks in patients with IPF and abnormal GER; correlate the reduction in acid and non-acid reflux events with the change in FVC over 48 weeks in patients with IPF and abnormal GER; determine the safety of laparoscopic anti-reflux surgery in patients with IPF and abnormal GER; explore the impact of laparoscopic anti-reflux surgery on key secondary endpoints over 48 weeks in patients with IPF and abnormal GER; identify molecular markers of IPF disease activity and gastroesophageal reflux in biological samples from patients with IPF and abnormal GER.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Confirmed diagnosis of idiopathic pulmonary fibrosis
  • Abnormal GER on 24-hour pH monitoring (DeMeester score > 14.7)
  • Able to provide informed consent
  • Willing to undergo laparoscopic anti-reflux surgery

排除标准

  • FVC < 50% predicted
  • FEV1/FVC ratio < 0.65
  • Resting room air PaO2 < 60mm Hg
  • Unable to walk 50 meters on 6 minute walk test
  • Acute respiratory illness in last 12 weeks
  • Experimental medication for IPF in last 28 days
  • Listed for lung transplantation at screening
  • Unable to safely undergo surgery
  • History of esophageal / bariatric / gastric surgery
  • History of cancer (other than non-melanoma skin cancer) in last 3 years
  • Pregnant at time of screening or enrollment
  • Unable to obtain pre-authorized approval from a third party payer for surgery and related costs
  • Life expectancy < 48 weeks due to another illness
  • BMI > 35
  • Known severe pulmonary hypertension (mean pressure > 35 mm Jg on RHC; RVSP > 50 mm Hg on ECHO)

结局指标

主要结局

Forced Vital Capacity (FVC)

时间窗: Baseline and 48 weeks

Change in FVC (in liters) between enrollment and 48 weeks.

次要结局

  • University of California San Diego (UCSD) Shortness of Breath Questionnaire (SOQB) Score(Baseline and 48 weeks)
  • 6-minute Walk Distance(Baseline and 48 weeks)
  • Change in Score From Baseline for Acid and Non-acid Reflux Events at 48 Weeks(Baseline and 48 weeks)
  • Safety of Laparoscopic Anti-reflux Surgery(48 weeks)
  • All-cause Mortality(48 weeks)
  • Non-elective Hospitalization(Baseline and 48 weeks)
  • Acute Exacerbations(Baseline and 48 weeks)
  • St. George's Respiratory Questionnaire (SGRQ) Score(Baseline and 48 weeks)
  • High-Resolution CT (HRCT) Fibrosis Score.(Baseline to 48 weeks)
  • Cough Visual Analog Scale (VAS)(Baseline and 48 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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