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
- Diseases
- High blood pressure
- 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
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| - Coordinator of this site? Confirm its status | Abu Dhabi | United Arab Emirates | Recruiting |
| - Coordinator of this site? Confirm its status | Dubai | United Arab Emirates | Recruiting |
| - Coordinator of this site? Confirm its status | Fujairah | United Arab Emirates | Recruiting |
| - Coordinator of this site? Confirm its status | Ras al-Khaimah | United Arab Emirates | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.