The Effect of Timing of Antihypertensive Medication on Diurnal Fluctuations in Blood Pressure Using a Wearable Sensor With Continuous Monitoring

Hypertension Clinical Trial

— ABPM  

Official title:

The Effect of Timing of Antihypertensive Medication on Diurnal Fluctuations in Blood Pressure Using a Wearable Sensor With Continuous Monitoring

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT04826250
• Other study ID #: ABPM
• Status: Withdrawn
• Phase: N/A
• Start date: January 1, 2021
• Est. completion date: June 1, 2022

Study information

• Verified date: February 2024
• Source: Tel Aviv University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Minimal or absent of diurnal fluctuation in blood pressure, and specifically conditions in which BP values are elevated during the night compared to daytime (rather than "nighttime dipping"), are associated with higher rates of morbidity and all-cause mortality. However, there is a gap in the scientific literature as to the optimal, individualized, timing of administration of antihypertensive drugs to balance daytime/nighttime fluctuations in BP to reduce the risk for cardiovascular morbidity and all-cause mortality.

To date, the most widely used method for semi-continuous, ambulatory monitoring of BP is a Holter, cuff-based monitor, which is cumbersome to use and therefore results in low patient compliance. Despite various attempts to overcome this problem, practical, patient-friendly methods for continuous BP monitoring throughout the day and night are currently not available.

Thus, the main of this study was to investigate whether there is a differential effect of timing of administration of antihypertensive drugs on diurnal fluctuations in BP using a wearable, cuff-less sensor with continuous monitoring capabilities. It is hypothesized that evening medication will improve BP fluctuations throughout the day (e.g., allow nighttime dipping and prevent morning surges) to a greater extend than morning meditation in people with hypertension.

Description:

Elevated blood pressure (i.e., hypertension) is a major risk factor for cardiovascular morbidity and all-cause mortality. Medical treatment can significantly improve the prognosis of those with hypertension. It has also been suggested that nighttime medication is more effective in improving mortality and morbidity compared to daytime medication. This hypothesis relates to the fact that lack of a reduction in BP during the night (termed "non-dipping") is associated with a worse prognosis, and therefore nighttime medication can potentially improve the desired diurnal fluctuations in BP and improve health outcomes in those with hypertension to a greater extent than daytime medication. However, whether the timing of drug administration affects the desired diurnal fluctuations in BP remains unknown.

To assess fluctuations in BP throughout the day, and specifically during the night, an ambulatory BP monitoring (ABPM) for 24 hours is required. Research suggests that this method allows classification of hypertension and thus more precise prediction of the patient's cardiovascular risk compared to office-based BP monitoring.

To date, clinician's ability to continuously monitor BP throughout the day has been limited, as the mostly commonly used method of Holter monitoring only allows for BP measurement every 30 min and imposes a significant burden on the patient. The latter limitation affects patients' compliance, and thus clinicians' ability to accurately assess daily BP fluctuations (or lack thereof) that present a major health risk factor.

Thus, the main aim of this study is to use a new wearable, cuff-less technology that that allows continuous ambulatory monitoring of BP to assess whether nighttime medication for hypertension improved diurnal fluctuations in BP to a better extent compared to daytime medication.

Methods:

This is interventional, cross-over and randomized study will be performed in a medical hospital. One hundred and fifty hypertensive patients, ages 30-80, will be recruited by a practicing medical physician and perform baseline tests that include blood work and BP measurement, as well as 24 monitoring of physiological signs (e.g., heart rate, BP, cardiac output and index and vascular resistance) using a photoplethysmogram (PPG)-based wireless, wearable device to obtain baseline measures. Participants will then begin medical treatment, either in the morning or evening, for four weeks. Physiological signs will again be continuously monitored using the wireless device during the last 48 hours of this time-period. After four weeks, participants will switch the timing of their medication for four more week, including 48 hours of monitoring.

Blood pressure measurement: BP will be continuously collected using a wearable, non-invasive, wireless chest-monitor (Biobeat Technologies Ltd., Petah Tikva, Israel), that is based on PPG technology. Systolic and diastolic BPs will be monitored and recorded continuously for the last 48 hours of each four-week intervention and compared between morning and evening medication, for each participant (i.e., each participant will serve as their own control).

Blood tests: Blood work will be performed after a 12-hour fast at baseline and at the end of each intervention. Measured parameters such as glucose, insulin, low and high density lipoprotein cholesterol, total cholesterol ,triglycerides sodium and potassium will enable assessment of cardio-metabolic risk.

Questionnaires: life quality and sleep quality questionnaires will be administered at baseline and at the end of each intervention

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: June 1, 2022
• Est. primary completion date: April 15, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 30 Years to 80 Years

Eligibility

Inclusion Criteria:

• Hypertension

Exclusion Criteria:

• hypertensive emergency

• Those taking more than 3 anti-hypertensive drugs

• congestive heart failure

• pregnancy

• renal failure

Related Conditions & MeSH terms

• Hypertension

Intervention

Procedure:
• Timing of medication
Either morning or nighttime medication

Locations

Country	Name	City	State
Israel	Sheba Medical Center	Tel HaShomer

Sponsors (1)

Lead Sponsor	Collaborator
Tel Aviv University

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Nighttime blood pressure	blood pressure measured during the night	Baseline
Primary	Nighttime blood pressure	blood pressure measured during the night	At the end of the first four-week intervention
Primary	Nighttime blood pressure	blood pressure measured during the night	At the end of the second four-week intervention
Primary	morning blood pressure	blood pressure measured during the morning hours	Baseline
Primary	morning blood pressure	blood pressure measured during the morning hours	At the end of the first four-week intervention
Primary	morning blood pressure	blood pressure measured during the morning hours	At the end of the second four-week intervention
Secondary	Blood Glucose	Blood parameters indicative of cardio-metabolic health	Baseline
Secondary	Blood Glucose	Blood parameters indicative of cardio-metabolic health	At the end of the first four-week intervention
Secondary	Blood Glucose	Blood parameters indicative of cardio-metabolic health	At the end of the second four-week intervention
Secondary	Insulin	Blood parameters indicative of cardio-metabolic health	Baseline
Secondary	Insulin	Blood parameters indicative of cardio-metabolic health	At the end of the first four-week intervention
Secondary	Insulin	Blood parameters indicative of cardio-metabolic health	At the end of the second four-week intervention
Secondary	Low and high density lipoprotein cholesterol, total cholesterol, triglycerides	Blood parameters indicative of cardio-metabolic health	Baseline
Secondary	Low and high density lipoprotein cholesterol, total cholesterol, triglycerides	Blood parameters indicative of cardio-metabolic health	At the end of the first four-week intervention
Secondary	Low and high density lipoprotein cholesterol, total cholesterol, triglycerides	Blood parameters indicative of cardio-metabolic health	At the end of the second four-week intervention
Secondary	Sodium, potassium	Blood parameters indicative of cardio-metabolic health	Baseline
Secondary	Sodium, potassium	Blood parameters indicative of cardio-metabolic health	At the end of the first four-week intervention
Secondary	Sodium, potassium	Blood parameters indicative of cardio-metabolic health	At the end of the second four-week intervention