COPD Exacerbation (AECOPD)

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Review clinical trials related to COPD Exacerbation (AECOPD). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

COPD Flare-Up Clinic After Severe Exacerbations

This prospective randomized controlled trial evaluates whether a specialized "COPD flare-up clinic service" improves outcomes in patients following an acute exacerbation of chronic obstructive pulmonary disease (AECOPD). Patients presenting to the emergency department with AECOPD and discharged or hospitalized will be randomized 1:1 to either structured follow-up in a dedicated flare-up clinic or standard follow-up by scheduled telephone interviews. The researches hypothesize that structured follow-up in a specialized clinic will reduce recurrent exacerbations, optimize long-term COPD management, and improve patients' quality of life compared to standard care.

Participants needed: 240
Trial details
Age: 40-80Biological sex: AllType: InterventionalSponsor: Tel-Aviv Sourasky Medical CenterUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Prior COPD diagnosis based on clinical and spirometry accepted criteria. [+3]

Symptomatic heart failure as the main reason for emergency department visit in t... [+2]

Status: Recruiting

Impact of a Multimodal Intervention on Antibiotic Prescribing for Respiratory Infections in Primary Care

Antimicrobial resistance (AMR), considered one of the greatest global threats by the WHO, justifies the development of initiatives to promote appropriate antibiotic use-especially in primary care, where most antibiotics in France are prescribed and where misuse remains common. We are proposing a cluster-randomized controlled trial to evaluate the effectiveness of a bimodal intervention combining: (1) improved communication about the circulation of respiratory viruses, and (2) strengthened collaborative practices between general practitioners and pharmacists through a multidisciplinary protocol aimed at verifying that prescribed treatment durations comply with guidelines. The study will include six primary care practices (24 physicians), with three practices in each study arm. The aim of this project is to assess whether the bimodal intervention can reduce the duration of antibiotic treatments for upper and lower respiratory tract infections. The first component (a "viral infection prescription" tool) focuses on reducing unnecessary treatment initiation, while the second (pharmacist-led review) aims to shorten excessive prescription durations.

Participants needed: 4,500
Trial details
Biological sex: AllType: InterventionalSponsor: University Hospital, CaenUpdated: Jan 22, 2026Locations: 1
Eligibility criteria

Not listed