Skip to content

Six Months Clinical and Echocardiographic Outcome of ARNI LCZ696 Therapy in HFrEF Patients

Six Months Clinical and Echocardiographic Outcome of Angiotensin Receptor-Neprilysin Inhibitor (ARNI) LCZ696 Therapy in Heart Failure Patients With Reduced Ejection Fraction (HFrEF)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03816306
Enrollment
100
Registered
2019-01-25
Start date
2018-06-01
Completion date
2019-12-01
Last updated
2020-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure With Reduced Ejection Fraction

Brief summary

To evaluate the clinical and echocardiographic outcome of LCZ696 therapy in HFrEF (NYHA Class II - IV and EF =≤ 40%).patients, in addition to the efficacy of LCZ696 in reducing mortality and rehospitalisation rate.

Interventions

LCZ696 is an Angiotensin receptor neprilysin inhibitor. It's composed of Sacubitril/Valsartan. LCZ696 starting dose 50 mg P.O. BID, LCZ696 100 mg P.O. BID and up-titration to LCZ696 200 mg P.O. BID.

Sponsors

Mohammed Alnims
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. ≥18 year old. 2. Functional class using New York Heart Association (NYHA) classification class II, III or IV %). 3. Left ventricular systolic dysfunction using transthoracic echocardiography with EF ≤ 40%. 4. Who was already taking ACE inhibitors or ARBs.

Exclusion criteria

1. Symptomatic hypotension. 2. Systolic blood pressure \<100 mm Hg. 3. Estimated glomerular filtration rate (eGFR) \<30 mL/min/1.73 m2. 4. History of angioedema. 5. Hisotry of unacceptable side effects while on while on treatment with an ACE-inhibitor or ARBs.

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants That Had Either Cardiovascular (CV) Death or Heart Failure (HF) Hospitalization.6 Months after starting LCZ696 TherapyNumber of participants that had either CV death or HF hospitalization due to HF.
Change From Baseline to Month 6 for The Minnesota Living with Heart Failure Questionnaire (MLHFQ).6 Months after starting LCZ696 TherapyChange From Baseline to Month 6 for the Minnesota Living with Heart Failure Questionnaire (MLHFQ). The questionnaire was designed as a self-administered measure of the effects of heart failure and treatments for heart failure on patients' quality of life. The questionnaire has 21 items assess the impact of frequent physical symptoms of heart failure and the effects of heart failure on physical and social functions. The response scale for all 21 items on the MLHF is based on a 6-point ( from 0 to 5 ). Scores are transformed to a range of 0-105, in which higher scores reflect better health status.

Secondary

MeasureTime frameDescription
Number of Patients - All-cause Mortality.6 Months after starting LCZ696 TherapyNumber of patients - All-cause mortality. All-cause mortality is common in HF patients.
Number of Patients With First Confirmed Renal Dysfunction.6 Months after starting LCZ696 TherapyNumber of patients with first confirmed renal dysfunction ( a decrease in the eGFR of at least 50% or a decrease of more than 30 ml per minute per 1.73 m2 to less than 60 ml per minute per 1.73 m2 ).
Number of Patients with Changes in The Left Ventricular Systolic Function (EF).6 Months after starting LCZ696 TherapyNumber of Patients with improvement in the ejection fraction.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026