Boosting Regional Integration for COP D Care Through Guided Implementation and Audit of Post Exacerbation Transition Bundle
Launched by ASTRAZENECA · Oct 16, 2024
Trial Information
Current as of June 09, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new approach to improve care for patients with Chronic Obstructive Pulmonary Disease (COPD) after they experience flare-ups, known as exacerbations. The research involves working with 36 hospitals to see if a specific care plan, called a "transition bundle," can help patients recover better and avoid future hospital visits. The trial will include about 1,368 patients aged between 40 and 80 who have been diagnosed with COPD and have had at least two moderate flare-ups or one severe flare-up in the past year.
To be eligible for the trial, participants should have a confirmed diagnosis of COPD and be able to provide consent to join. Importantly, those who have been on a specific type of inhaler treatment for a long time, or have stable COPD symptoms, may not qualify. If you choose to participate, you can expect to receive care that aligns with the new approach being tested, which aims to help improve your overall health and manage your COPD more effectively. This trial is currently recruiting participants and welcomes all genders.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Diagnosed COPD (post- bronchodilator FEV1/FVC \< 0.7)
- • 40\~80 years
- • CAT≥10
- • At least two moderate or at least one severe exacerbation history in past 1 year
- • Able to sign informed consent
- Exclusion Criteria:
- • Continuous triple inhalation therapy for ≥6 months at baseline (include single inhaler and multiple inhalers)
- • Stable COPD (symptom such as cough, sputum and shortness of breath are mild or stable, clinical condition has basically returned to pre-exacerbation)
- • Comorbidities require/contraindicate long-term use of glucocorticoid treatment: asthma, interstitial lung disease, sarcoidosis, cystic fibrosis, active tuberculosis recurrent aspiration pneumonia ect.
- • Serious comorbidities threaten to life expected survival time no more than 1 year: severe heart disease, severe chronic liver, severe kidney disease, cerebrovascular disease with long-term bed rest and malignant tumours ect.
- • Not living in the healthcare area
- • Patients currently participating in any other interventional studies
About Astrazeneca
AstraZeneca is a global biopharmaceutical company dedicated to the discovery, development, and commercialization of innovative medicines across various therapeutic areas, including oncology, cardiovascular, respiratory, and autoimmune diseases. With a strong commitment to scientific research and patient-centric solutions, AstraZeneca leverages cutting-edge technology and a robust pipeline to address unmet medical needs. The company collaborates with healthcare professionals, academic institutions, and other organizations to advance clinical trials and deliver transformative therapies, aiming to improve health outcomes and enhance the quality of life for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Beijing, , China
Hangzhou, , China
Hefei, , China
Changsha, , China
Suzhou, , China
Wenzhou, , China
Nanchang, , China
Jining, , China
Chenzhou, , China
Neijiang, , China
Langfang, , China
Chifeng, , China
Yichang, , China
Fuyang, , China
Xinyang, , China
Deyang, , China
Nanchong, , China
Xiangtan, , China
Anyang, , China
Baise, , China
Chuzhou, , China
Langzhong, , China
Qiannan, , China
Qujing, , China
Sanmenxia, , China
Shaoyang, , China
Tengzhou, , China
Tieling, , China
Xiaogan, , China
Yuling, , China
Zaoyang, , China
Bijie, , China
Jieyang, , China
Jiujiang, , China
Kaiyuan, , China
Leping, , China
Yancheng, , China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported