Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06825728

Metoprolol in Patients With HFrEF and COPD

Metoprolol in Patients With Heart Failure With Reduced Ejection Fraction and Chronic Obstructive Pulmonary Disease

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
311 (estimated)
Sponsor
Xiangya Hospital of Central South University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of the clinical trial was to see if Metoprolol was effective in treating patients with heart failure and chronic obstructive pulmonary disease. It will also learn about the safety of Metoprolol. The main questions it aims to answer are: Did Metoprolol reduce the frequency of all-cause deaths and re-hospitalizations in subjects? What medical problems do participants experience after taking Metoprolol? The researchers will compare different doses of Metoprolol to see the best dose for Metoprolol. Participants will: Take Metoprolol 23.75mg/ day or the maximum tolerable dose of Metoprolol daily for 24 months. Regular outpatient follow-up visits to the research center. Their symptoms and Metoprolol dosage were recorded.

Conditions

Interventions

TypeNameDescription
DRUGDifferent doses of Metoprolol.The control group received 23.75mg/d of metoprolol, and the experimental group received the maximum tolerable dose of metoprolol.

Timeline

Start date
2025-02-01
Primary completion
2028-02-01
Completion
2028-02-01
First posted
2025-02-13
Last updated
2025-02-13

Source: ClinicalTrials.gov record NCT06825728. Inclusion in this directory is not an endorsement.