Nighttime blood pressure pattern may reveal hidden heart risks
NCT ID NCT07200856
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at whether the natural drop in blood pressure during sleep (called 'dipping') is linked to changes in the heart's electrical activity in people with high blood pressure. Researchers will monitor 140 adults using a 24-hour blood pressure device and compare those whose blood pressure dips enough at night to those whose does not. The goal is to see if a lack of nighttime dipping is tied to higher risk for dangerous heart rhythms, which could help doctors better assess heart risk in the future.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors better identify hypertensive patients at higher risk for heart problems based on their nighttime blood pressure patterns.
- What could go wrong
- This is an observational study, not a treatment trial. It will not directly change patient care, and results may not apply to all patient groups.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 140 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult patients (≥18 years) with essential hypertension attending the Cardiology Department at Assiut University Heart Hospital. All participants will undergo 24-hour ambulatory blood pressure monitoring, electrocardiography, and echocardiography to classify them into dipper and non-dipper groups
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults ≥18 years old * Diagnosed with essential hypertension * Completed 24-hour ambulatory blood pressure monitoring (ABPM) * Availability of good-quality 12-lead ECG * Availability of good-quality transthoracic echocardiography Exclusion Criteria: * Body mass index (BMI) \> 34.9 kg/m² * Atrial fibrillation or atrial flutter * Use of QT-prolonging medications * End-stage renal disease or liver failure * Bundle branch block or presence of pacemaker * Prior coronary revascularization (PCI or CABG) * Significant electrolyte imbalance
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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