Fact CheckerSign in

NCT07465666Recruiting

A Real-world Study of the Effectiveness of Angiotensin Receptor-Neprilysin Inhibitor Therapy in Hypertensive Patients in the United Arab Emirates

Real-world Effectiveness of Angiotensin Receptor-Neprilysin Inhibitor (ARNi) Therapy in Lowering Blood Pressure in Hypertensive Patients in the United Arab Emirates

Source: ClinicalTrials.gov · Last updated 21 Oct 2026

Brief summary (registry, in English)

The aim of this study is to evaluate the real-world effectiveness of ARNi (sacubitril/valsartan) therapy and antihypertensive monotherapy in reducing blood pressure in hypertensive patients residing in the United Arab Emirates. Antihypertensive monotherapies will include angiotensin-converting enzyme (ACE) inhibitors, angiotensin II receptor blockers (ARBs), and calcium channel blockers (CCBs).

Status (registry)
Recruiting
Study type
Observational
Enrollment
500 (estimated)
First submitted
6 Mar 2026
Start date
Oct 2026
Primary completion date
Aug 2027
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT07465666

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From Oct 2026 to the primary completion date, Aug 2027
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with malignant or severe hypertension (systolic blood pressure \[SBP\] ≥180 mmHg, diastolic blood pressure \[DBP\] ≥110 mmHg) at baseline.
  • Patients with secondary causes of hypertension, as determined by the treating physician.
  • Patients with a history of, or at risk of developing, angioedema.

Lab values

  • Patients with evidence of severe renal impairment (e.g., estimated glomerular filtration rate \[eGFR\] \<30 mL/min/1.73 m\^2).
  • Patients with serum potassium level ≥5.5 mmol/L at baseline.

Other

  • Pregnant or lactating women.

Who the study is looking for

  • Adult male or female patients (≥18 years).
  • Patients with physician-diagnosed hypertension (as defined by international guidelines including the American Heart Association/American College of Cardiology \[AHA/ACC\] guidelines and/or the 2024 European Society of Cardiology \[ESC\] guidelines).
  • Patients with documented office blood pressure ≥130/80 mmHg prior to initiating treatment (ARNi or monotherapy) or transitioning from monotherapy to ARNi.
  • Patients who are either antihypertensive therapy naïve or currently receiving antihypertensive monotherapy (ACE inhibitor/ARB/CCB) with a physician-directed requirement to transition to ARNi.
    • Note: Patients who transition from one monotherapy to another during the study are not eligible for inclusion.
  • Patients willing to provide written informed consent to participate in the study.

Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
Abu DhabiUnited Arab EmiratesRecruiting
-
Coordinator of this site? Confirm its status
DubaiUnited Arab EmiratesRecruiting
-
Coordinator of this site? Confirm its status
FujairahUnited Arab EmiratesRecruiting
-
Coordinator of this site? Confirm its status
Ras al-KhaimahUnited Arab EmiratesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.