About this trial
This study aims to explore a new therapeutic approach: the feasibility, safety and preliminary efficacy of directly spraying GM-CSF into the airway through bronchoscopy for the treatment of aPAP.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age: 18 to 60 years old;
Disqualifiers
Secondary PAP (such as secondary to blood diseases, etc.);
Patients with obvious pulmonary fibrosis, emphysema or irreversible lung function impairment;
Patients in the acute exacerbation stage;
Patients with other lung diseases (such as active pulmonary tuberculosis, bronchiectasis with purulent infection or other chronic infections; Have severe asthma, chronic bronchospasm, etc.
Trial design
Single group
Treatments tested in this trial
GM-CSF (granulocyte-macrophage colony-stimulating factor)
DrugBronchoscopy under general anesthesia or sedation; The predetermined dose of recombinant GM-CSF was dissolved in normal saline. The diseased lung segments were located through bronchoscopy and the liquid medicine was sprayed.
Treatment groups
Trial outcomes
Primary outcomes
Chest HRCT
Locations
Sponsors and contacts
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Jiuwu Bai
Lead sponsor
Shanghai Pulmonary Hospital, Shanghai, China
Sponsor institution
This trial is not recruiting at the moment. You can still explore other options: