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RecruitingNCT06769269Updated Jan 24, 2025

Hypertension Registry: Study of Primary and Secondary Hypertension Phenotypes, Complications, and Treatment Personalization.

An observational study in Arterial Hypertension, sponsored by Moroccan Society of Cardiology. Recruiting at 5 sites in Morocco. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-01-24.

Sponsored by Moroccan Society of Cardiology · Observational

From the registry’s dates

  • Primary completion was expected by Jan 2026, 9 months ago, but the record still lists the study as recruiting.
  • Started Jan 2025; still recruiting 1 year 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
10,000
Ages
18 Years and older
Sex
All
01

Study summary

The quality of primary healthcare systems for patients with hypertension (HTA) in Morocco is a critical issue due to its high prevalence and significant impact on morbidity and mortality. The concept of "quality in primary care" encompasses fundamental aspects such as timeliness, accessibility, and the provision of care based on current clinical guidelines and recommendations from professional societies.

This observational study on hypertension (HTA) uses an electronic registry accessible remotely to collect medical data from primary care and hospital settings. Investigators will be trained to ensure standardization in blood pressure measurements to minimize errors. The registry will include clinical, therapeutic, and complication data for patients aged 18 and over with a confirmed diagnosis of HTA, with information transmitted anonymously via a certified secure channel.

Informed consent from patients will be required for including their data in the registry. Collected data will include anthropometric measurements (weight, height, waist circumference, body mass index), blood pressure measurements by validated devices or ambulatory measurements, and metabolic assessments (blood glucose, total cholesterol, triglycerides, LDL, HDL, urea, creatinine, uric acid, urine albumin-to-creatinine ratio). Cardiovascular complications will also be recorded.

The study design is a cohort study with a cross-sectional perspective and a targeted follow-up period of one year. The study aims to evaluate the prevalence and phenotypes of HTA in Morocco, as well as the geographic distribution of the disease. It will compare current data with those from previous years and other North African countries to assess the applicability of Moroccan clinical practices and recommendations from the European Society of Cardiology (ESC). The goal is to enhance the understanding and management of HTA, as well as to optimize prevention and treatment strategies.

This comprehensive analysis will help identify potential gaps in primary care and develop strategies to improve the management of hypertensive patients. The comparative evaluation of data related to examinations, treatments, and complications of the cohort of patients followed for hypertension during the period 2024-2026, in comparison with results from previous years and other countries, will provide valuable insights into the shortcomings and progress in care delivery. This approach will not only identify areas needing improvement but also highlight significant advances in hypertension management.

02

Conditions studied

  • Arterial Hypertension

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03

In context

Hypertension

6,114 studies on the registry are indexed under Hypertension; 912 are open to participants now.

This study's planned enrollment of 10,000 is above the median of 350 across 1,163 observational studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

Moroccan Society of Cardiology is the lead sponsor of 2 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients will be recruited from various public and private research centers, whether they are already under follow-up for hypertension or newly diagnosed. Various specialists will be involved in the registry to increase the diversity of recruited patients, including cardiologists, general practitioners, and nephrologists. The objective is also to identify best practices for managing hypertension.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Individuals aged over 18 years.
  • Patients with blood pressure:

    • Higher than 140 mmHg systolic and/or higher or equal to 90 mmHg diastolic in consultation or in a hospital setting.
    • Higher than 135/85 mmHg at home or in ambulatory blood pressure measurements (ABPM).
  • Patients who have agreed and signed the .
  • Patients with legal status in the Moroccan kingdom.

Exclusion criteria

Exclusion Criteria:

  • Patient without diagnosis of hypertension
  • Patient under 18 years old
  • Patients refusing to sign the .
  • Patients with illegal status in the kingdom.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
10,000 participants (estimated)
Target follow-up
1 Year
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. Prevalence of arterial hypertension

    Proportion of population with arterial hypertension in Morocco.

    Time frame: At inclusion

  2. To assess the distribution of HTA across the kingdom

    Analyzing how arterial hypertension is spread geographically and demographically within the kingdom.

    Time frame: At inclusion

  3. To analyze the various phenotypes of primary and secondary hypertension as well as the associated complications

    Studying the different forms or presentations of hypertension (both primary and secondary) and their related health impacts, such as organ damage or cardiovascular events.

    Time frame: At inclusion

  4. Causal relationships between Arterial Hypertension and various complications

    Causal relationships between arterial hypertension and various complications such as myocardial infarction, heart failure, atrial fibrillation, renal failure, and stroke, as well as links between arterial hypertension and other secondary pathologies

    Time frame: At inclusion

Secondary outcomes

  1. Collect information on complications related to arterial hypertension after 1 year

    Time frame: 1 year

07

Study locations

5 of 5 sites recruiting
  • Moroccan Society of Cardiology
    Casablanca, Morocco
    Recruiting
  • UM6SSP
    Casablanca, Morocco
    Recruiting
  • Moroccan Society of Cardiology
    Meknès, Morocco
    Recruiting
  • Ibn Sina Hospital Center
    Rabat, Morocco
    Recruiting
  • Mohamed V Military Hospital
    Rabat, Morocco
    Recruiting
    • Najat MOUINE · Contactmouine2@yahoo.fr · +212661202733
    • Najat MOUINE · Contact
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 24, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06769269
Lead sponsor
Moroccan Society of Cardiology
Collaborators
F&C Clinical Trials
Responsible party
Sponsor
First posted
Jan 10, 2025
Start date
Jan 21, 2025
Primary completion
Jan 21, 2026 (estimated)
Completion
Jan 21, 2027 (estimated)
Last update
Jan 24, 2025

Study contacts

F&C Clinical Trials
Contact
infos@fc-ct.com
+33 7 69 27 88 10

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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