评估新型联合治疗方案(D组)与标准治疗用于脓肿分枝杆菌肺病强化期治疗的FORMaT适应性平台试验
该数据集来自 clinicaltrials.gov,主题为脓肿分枝杆菌肺病(MABS-PD)的强化期治疗研究,属于呼吸系统疾病/肺结核分类

基本信息
资源简介
评估新型联合治疗方案(D组)与标准治疗用于脓肿分枝杆菌肺病强化期治疗的FORMaT适应性平台试验
该数据集来自 clinicaltrials.gov,主题为脓肿分枝杆菌肺病(MABS-PD)的强化期治疗研究,属于呼吸系统疾病/肺结核分类。覆盖条件包括脓肿分枝杆菌肺病、脓肿分枝杆菌感染、非结核分枝杆菌(NTM)感染及非结核分枝杆菌肺病。研究在FORMaT适应性平台试验中,比较新型联合方案(Arm D)与标准治疗在伴或不伴囊性纤维化人群中的强化期治疗效果。数据可用于了解该罕见且难治性肺部感染的临床试验设计、治疗方案与人群特征(来源 clinicaltrials.gov)。
【数据内容】
源站描述(机器翻译,仅供参考):Conditions: Mycobacterium Abscessus Pulmonary Disease, Mycobacterium Abscessus Infection, Non-Tuberculous Mycobacterial (NTM) Infections, Non-Tuberculous Mycobacteria Pulmonary Disease. 脓肿分枝杆菌肺病(MABS-PD)是一种罕见且严重的肺部感染,影响已有肺部问题(如支气管扩张、囊性纤维化、既往结核病或免疫系统减弱)的人群,也影响没有既存肺部问题的人群。这种感染在全球范围内日益常见,且因对多种抗生素高度耐药而难以治疗。当前治疗通常持续12-18个月,患者难以耐受,且常引起显著副作用。本研究将测试在治疗最初四周(即“强化期”)给予的一种新型抗生素联合方案。该新方案包括静脉注射舒巴坦-杜
【主题与分类】
主题标签:Mycobacterium Abscessus Infection。本站分类:呼吸系统疾病/肺结核。
【获取与许可】
源站页面:https://clinicaltrials.gov/study/NCT07485010
下载信息
注册下载
需要注册 Kaggle 账号并登录后下载,适合需要跟踪下载记录和使用 API 的用户。
暂未开放公开下载
无需注册即可直接获取公开样本或文档,适合快速预览和评估数据集质量。
免登录有偿下载
公开数据集受托下载与技术交付服务。
提供高速下载与技术交付服务(收技术服务费,非数据销售)
暂未开放当前数据集主要来源为 Kaggle 公开托管,完整影像包建议通过原始链接或 Kaggle API 获取。
使用方式
数据集获取
源站:https://clinicaltrials.gov/study/NCT07485010
标准获取流程:
- 访问源站链接,注册/登录账号;
- 进入数据集详情页,按页面指引申请权限或直接下载;
- 部分平台提供 SDK,例如:
- OpenDataLab:
pip install openxlab后openxlab.dataset.get(...) - ModelScope:
pip install modelscope后modelscope download - 天池: 登录后页面提供直链下载
以源站「数据下载/使用文档」页面为准。
- OpenDataLab:
数据说明
Conditions: Mycobacterium Abscessus Pulmonary Disease, Mycobacterium Abscessus Infection, Non-Tuberculous Mycobacterial (NTM) Infections, Non-Tuberculous Mycobacteria Pulmonary Disease. Mycobacterium abscessus pulmonary disease (MABS-PD) is a rare and serious lung infection that affects people who already have lung problems such as bronchiectasis, cystic fibrosis, past tuberculosis, or weakened immune systems, as well as people who do not have pre-existing lung problems. This infection is becoming more common worldwide and is difficult to treat because it is highly resistant to many antibiotics. Current treatment usually lasts 12-18 months, is hard for patients to tolerate, and often causes significant side effects. This study will test a new combination of antibiotics given during the first four weeks of treatment-the “intensive phase.” The new regimen includes intravenous sulbactam-durlobactam and intravenous ceftriaxone, along with oral amoxicillin, oral azithromycin, and oral clofazimine. The trial will compare this new approach to the current standard-of-care therapy using the existing FORMaT adaptive platform trial, which was created to identify better treatments for MABS-PD. The main goal of the study is to find out whether the new combination can clear the infection while also being easier for patients to tolerate. Additional study measures will look at lung function, chest imaging, quality of life, and health-care use. The trial also includes several research components that will examine how the drugs behave in the body, immune responses, mycobacterial genetics, and antibiotic resistance. This innovative study aims to provide the first high-quality clinical evidence for a potentially more effective and less toxic treatment option for people living with this challenging and severe lung infection.
数据加载示例(图像类)
from PIL import Image
import glob, os
files = (glob.glob(os.path.join(path, "**", "*.png"), recursive=True)
+ glob.glob(os.path.join(path, "**", "*.jpg"), recursive=True)
+ glob.glob(os.path.join(path, "**", "*.tif"), recursive=True))
print("图像文件数:", len(files))
img = Image.open(files[0]); print("尺寸/模式:", img.size, img.mode)
# torchvision Dataset 方式:
# from torchvision import datasets
# ds = datasets.ImageFolder(path) # 要求 子目录=类别
目录组织与标注格式以源站说明和下载后实际文件为准。
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