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

M

Mohammed Alnims

Status

Completed

Conditions

Heart Failure With Reduced Ejection Fraction

Treatments

Drug: LCZ 696

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

100 participants in 1 patient group

Single group study
Treatment:
Drug: LCZ 696

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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