Actively Recruiting

Phase Not Applicable
Age: 21Years - 80Years
All Genders
ID06938633

Utility of Urine Mass Spectrometry Analysis in Addressing Medication Non-adherence in Patients With Poorly Controlled Hypertension

Led by Changi General Hospital · Updated on 2025-04-22

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Hypertension is a major cause of cardiovascular disease and death, and many patients have uncontrolled blood pressure often due to not taking medications as prescribed. This research aims to study if testing urine for antihypertensive drugs can better detect medication non-adherence in patients with hypertension, including those who recently had a stroke. The study will evaluate whether identifying non-adherence and providing targeted counseling can improve medication use and blood pressure control. The study has three parts: first, reviewing urine samples from 200 patients who recently had a stroke to check medication adherence; second, enrolling 100 patients with poorly controlled hypertension to assess adherence prospectively; and third, counseling participants found to be non-adherent and reassessing them at 3 and 6 months. Urine samples of 50ml will be collected during visits for mass spectrometry analysis to detect medication levels. Participants will attend study visits at enrollment, 3 months, and 6 months, providing urine samples each time. Researchers will measure changes in medication adherence rates and blood pressure, including systolic and diastolic values, over 6 months. The study aims to improve adherence and blood pressure control, potentially reducing healthcare visits and serious cardiovascular events.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 21Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age of 21 to 80 years
  • Systolic blood pressure of 140 mmHg or higher, or average systolic blood pressure of 135 mmHg or higher, or diastolic blood pressure of 90 mmHg or higher, or average diastolic blood pressure of 85 mmHg or higher, based on at least two measurements
  • Currently taking two or more hypertension medications
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Significant kidney impairment with eGFR less than 45 mL/min/1.73m2 or on dialysis
  • Known history of chronic liver disease

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 months

Participants provide urine samples to assess medication adherence and receive counseling if non-adherence is detected.

3 visits (in-person) at enrollment, 3 months, and 6 months

Trial Site Locations

Total: 1 location

1

Changi General Hospital

Singapore, Singapore

Actively Recruiting

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Research Team

S

Sumitro Harjanto, MD MRCP

G

Geraldine Lim

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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