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临床试验/NCT05331729
NCT05331729已完成1 期

Evaluation of the Value of 18F-Fluoromisonidazole (18F-FMISO) Positron Emission Tomography Hypoxia Imaging in Idiopathic Pulmonary Fibrosis - a Non-randomized Proof-of-concept Study Comparing Patients with Idiopathic Pulmonary Fibrosis and Healthy Subjects

Centre Hospitalier Universitaire Dijon2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年3月20日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
20
试验地点
2
主要终点
Lung SUVmean of 18F-FMISO measured in PET

研究概览

简要总结

Idiopathic pulmonary fibrosis (IPF) is a rare, chronic, lethal disease of unknown etiology and with a variable course. There is currently no test in routine care that can assess both the anatomical and functional damage of the disease at an early stage. This is the first human study in IPF to evaluate the value of a non-invasive tracer, 18F-fluoromisonidazole (18F-FMISO), targeting hypoxia in IPF patients.

This is a Phase I, proof-of-concept, single-center, open-label, parallel group study.

It will include 2 groups:

  • 1 group of 10 IPF patients
  • 1 group of 10 healthy volunteers matched to IPF patients for age and gender

研究设计

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

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • For all patients (IPF and healthy volunteers) :
  • Person who has given written consent
  • Age ≥ 50 years
  • Absence of disease, comorbidity, or treatment that may interfere with the evaluation of the study objective, as decided by the investigator
  • For patients with IPF only:
  • Diagnosis of IPF according to the criteria of the current international recommendations (ATS/ERS/JRS/ALAT of 2011) and validated in a multi-disciplinary meeting in a Competence or Reference Center
  • Patients who have had a high-resolution thoracic CT scan less than 1 month previously as part of the management of their disease
  • Patients who have had a PFT less than 1 month previously as part of the management of their disease
  • For healthy volunteers only:
  • Absence of functional respiratory signs - absence of dyspnea on exertion and at rest and absence of chronic cough.
  • Normal clinical examination with no crackles on pulmonary auscultation
  • No personal history of chronic hypoxemic respiratory disease

排除标准

  • Person who is not covered by national health insurance
  • Cancer or history of cancer in the past 5 years (except basal cell skin cancer)
  • Chronic lung disease other than IPF or a history incompatible with the diagnosis of idiopathic pulmonary fibrosis (thoracic radiotherapy, pneumotoxic chemotherapy, etc.)
  • Exacerbation of IPF during treatment
  • Active smoking
  • Patient requiring long-term oxygen therapy (excluding ambulatory oxygen therapy alone)
  • Contraindication to PET or CT scan or presence of a condition disturbing the interpretation :
  • known allergy to 18F-FMISO
  • pregnancy or breastfeeding
  • claustrophobia
  • uncontrolled type I/II diabetes (HbA1c >7%)
  • surgical intervention in the previous month
  • Radiotherapy session in the previous 3 months
  • concomitant granulomatous condition (sarcoidosis type) or pulmonary inflammation
  • Moderate or severe renal insufficiency (GFR < 70 ml/min/1.73 m²)
  • Person under legal protection (curatorship, guardianship)
  • Adult unable to express consent
  • SECONDARY EXCLUSION CRITERIA only for healthy volunteers
  • Abnormal 6 min walk test at screening
  • Abnormal PFT at screening with FVC ≤ 80% of predicted value and DLCO ≤ 75% of predicted value

结局指标

主要结局

Lung SUVmean of 18F-FMISO measured in PET

时间窗: At baseline

Comparison in IPF patients and healthy volunteers

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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