Clinical Trials Directory

Trials / Completed

CompletedNCT05799638

Strategy, Efficacy and Safety of Medication Usage in Heart Failure Patients Who Were Intolerable to GDMT

Medication Strategies in Heart Failure Patients Who Are Intolerable to Guideline-directed Medical Therapy

Status
Completed
Phase
Study type
Observational
Enrollment
263 (actual)
Sponsor
Chongqing Medical University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

SEMI trial is a single-center, real-world based prospective cohort study. The study enrolled acute heart failure patients admitting to the hospital and intended to accept heart failure therapy. The current guideline recommend ACEI/ARB/ARNI, β blocker, SGLT2i and MRA as the cornerstone medication of HFrEF therapy, but a part patients were intolerable to GDMT because of hypotension, hyperkalemia or renal insufficency. Vericiguat is a new medication therapy choice for the patients with heart failure with reduced ejection fraction (HFrEF), it may has less influence on blood pressure, it is unkonwn about the efficacy and safety of vericiguat in patients who were intolerable to GDMT.

Detailed description

The study aim to provide evidence of medication strategy in heart failure patients, especially for patients who are intolerable for GDMT.

Conditions

Interventions

TypeNameDescription
OTHERGuideline-Directed Medication Treatment (GDMT)GDMT contains ACEIs/ARBs/ARNI, β blockers, SGLT2is, MRAs. ACEI/ARB/ARNI and β blocker will gradually be titrated up to the maximum tolerable dose

Timeline

Start date
2023-01-01
Primary completion
2023-12-31
Completion
2024-06-30
First posted
2023-04-05
Last updated
2024-08-01

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05799638. Inclusion in this directory is not an endorsement.