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Clinical Trials in Singapore / NCT06938633
Recruiting Not applicable

Addressing Medication Non-adherence in Patients With Poorly Controlled Hypertension Using Urine Mass Spectrometry

NCT06938633 · tracked via the Priya Life Science Singapore tracker
Phase
Not applicable
Started
2024-02-07
Last updated
2025-04-22

Condition(s) studied

HypertensionUncontrolled HypertensionNon-Adherence, Medication

Investigational drug(s) / intervention(s)

mass spectrometry analysis

mass spectrometry analysis: The collected urine samples will be analyzed to determine medication adherence during study visits

Study summary

* Hypertension is the single largest contributor to cardiovascular disease and death. While adequate control of hypertension reduces risk of disease, many patients have uncontrolled hypertension. This is often due to medication non-adherence. Left undetected, patients are prescribed additional medications, and referred to multiple specialists for investigations - leading to increased healthcare costs. Hence, detecting non-adherence to antihypertensive medications is important. However, patient history, patient recall, or questionnaires, are often inaccurate. Most recently, urine measurements of antihypertensive drug levels, using mass spectrometry, has been established as the gold standard to assess medication adherence. The one-time urine test for medication adherence is ideal: It's convenient, non-invasive, economical, and can be easily performed in a clinic setting. By improving blood pressure control, this will lead to reductions in healthcare visits, avoidance of catastrophic cardiovascular events. Ultimately, this translates to significant economic savings for both patients with hypertension and the healthcare system.
* Therefore, the investigators hypothesize that the implementation of urine adherence testing coupled with targeted counselling will improve the adherence and blood pressure control in hypertension. To do this, the investigators aim to (1) evaluate for medication adherence in 312 participants with recent stroke and hypertension; (2) evaluate for medication non-adherence in participants with uncontrolled hypertension; and (3) assess if detection of non-adherence can improve hypertension control.

Eligibility

Sex
ALL
Min age
21 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age of 21 - 80 years 2. Systolic blood pressure of ≥140 mmHg or average systolic blood pressure ≥135 mmHg, or diastolic blood pressure ≥90 mmHg or average diastolic blood pressure ≥85 mmHg, on at least two measurements 3. Currently taking 2 or more hypertension medications 4. Able to provide informed consent. Exclusion Criteria: * Significant kidney impairment with eGFR of less than 45mL/min/1.73m2 or on dialysis * Known history of chronic liver disease

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Changi General Hospital Singapore Singapore Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06938633 on ClinicalTrials.gov ↗ ← All trials in Singapore