跳至主要内容
临床试验/NCT05270850
NCT05270850Unknown不适用

Clinical Study on Autologous Stromal Vascular Fraction(SVF) Treatment for Benign Airway Stenosis and Respiratory Tract Fistula

Guangzhou Institute of Respiratory Disease1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2022年3月20日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
20
试验地点
1
主要终点
Cure rate for benign airway stenosis

研究概览

简要总结

Benign airway stenosis and respiratory tract fistula are common types of airway injury. The diseases occurred after endogenous and exogenous stimuli (tuberculosis, tumor, surgery, tracheal intubation) causing damage to the airway mucosa, resulting in scar repair and irreversible loss of airway epithelium. Autologous adipose vascular fraction (stromal vascular fraction, SVF) is a mixture of cells obtained from adipose tissue through digestion and centrifugation, containing a variety of cell types, such as mesenchymal cells, endothelial progenitor cells, endothelial cells, pericytes, and macrophages. Previous studies have shown that SVF can achieve regeneration and wound healing through modulating the immune microenvironment, promoting angiogenesis, thereby promoting endogenous regeneration of the in situ adult stem cells. This project utilizes the tissue repair function of autologous SVF to treat benign airway stenosis and respiratory tract fistula. To clarify the efficacy and safety of autologous SVF in the treatment of airway injury.

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

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects aged between 18 to 75
  • Subjects diagnosed with benign airway stenosis, tracheoesophageal fistula(the sizes of the fistulas less than 2cm), and bronchopleural fistula
  • Subjects willing to accept SVF treatment
  • Subjects tolerant to the bronchoscope
  • Subjects signed informed consent

排除标准

  • Subjects with the following pulmonary diseases: asthma, active pulmonary tuberculosis, pulmonary embolism, pneumothorax, pulmonary hypertension, etc;
  • Subjects with incomplete remission of malignant tumors or with incurable malignant tumors;
  • Subjects with uncontrolled systemic infection;
  • Subjects requiring anti-clotting drugs;
  • Subjects with myocardial infarction, unstable angina, liver cirrhosis, acute glomerulonephritis, etc;
  • Subjects with syphilis, HIV, HBV, HCV antibody positive;
  • Subjects with Coagulation disorders such as hemophilia, giant platelet syndrome, thromboasthenia, etc;
  • Subjects with severe renal damage, serum creatinine is more than 1.5 times the upper limit of the normal value;
  • Subjects with liver disease or liver damage: ALT, AST, total bilirubin > 2 times the upper limit of the normal value;
  • Subjects with a history of psychosis or suicide or epilepsy or other central nervous system diseases;
  • Subjects with severe arrhythmias(e.g. ventricular tachycardia, frequent supraventricular tachycardia, atrial fibrillation, atrial flutter, etc.) or degree II above abnormal conduction;
  • Subjects allergic to thrombin;
  • Subjects accepted by any other clinical study within the first three months of the study;
  • Subjects with poor compliance;
  • Any other conditions might increase the risk of the patient or interfere with the clinical study.

结局指标

主要结局

Cure rate for benign airway stenosis

时间窗: within 3 months after administration

The proportion of patients who is no need for endotracheal intervention and with stable clinical symptoms after SVF treatment

Cure rate for respiratory tract fistula

时间窗: within 3 months after administration

The proportion of patients who have complete closure of fistula, no need for endotracheal intervention and with stable clinical symptoms after SVF treatment

次要结局

  • Times of unplanned treatment(within 3 months after administration)
  • Incidence of complications associated with SVF treatment(within 3 months after administration)
  • Clinical complete remission time(within 3 months after administration)

研究者

发起方
Guangzhou Institute of Respiratory Disease
申办方类型
Other
责任方
Principal Investigator
主要研究者

ShiYue Li

Director of Department of Respiratory Medicine

Guangzhou Institute of Respiratory Disease

研究点 (1)

Loading locations...

相似试验