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Clinical Trials in China / NCT07357012
Starting soon Observational

A Smart Wearable Device for Monitoring Urination Function in Benign Prostatic Hyperplasia

NCT07357012 · tracked via the Priya Life Science China tracker
Sponsor
Peking University Third Hospital
Phase
Observational
Started
2026-01-15
Last updated
2026-01-21

Condition(s) studied

Benign Prostatic Hyperplasia

Investigational drug(s) / intervention(s)

Electrical Impedance Tomography (EIT) Wearable Monitoring Device

Electrical Impedance Tomography (EIT) Wearable Monitoring Device: A non-invasive, portable device that uses an array of surface electrodes placed on the lower abdomen to measure bioimpedance changes. It reconstructs real-time, three-dimensional images and volume data of the bladder during filling and voiding phases.

Study summary

Benign Prostatic Hyperplasia (BPH) is a common condition that can cause bothersome urination problems and reduce quality of life. Accurately measuring how the bladder empties is important for diagnosis and treatment, but current methods like uroflowmetry can be inconvenient and are done only at a clinic.

This study aims to test a new, non-invasive smart wearable device that uses Electrical Impedance Tomography (EIT) to monitor bladder function in patients with BPH. The device is worn on the lower abdomen. In this study, participants will use this EIT device while also undergoing the standard uroflowmetry test. The main goal is to see how well the measurements from the new device (like urine flow rate and volume) agree with those from the standard test.

The study hopes to show that this wearable device can accurately and comfortably track bladder function over time. If successful, it could lead to a new tool for doctors to better monitor patients with BPH, even potentially at home.

Eligibility

Sex
MALE
Min age
Max age
Healthy volunteers
No
Inclusion Criteria: Patients with BPH who need urodynamic tests to further evaluate the underlying pathophysiology of LUTS prior to invasive treatment. Patients who understand and agree with the written informed consent, and voluntary to participate in the study. Exclusion Criteria: Patients with catheter-dependent urinary retention. Patients who cannot void \> 150ml. Patients with uncontrolled acute urinary tract infections. Patients who suffer from severe mental illness or other diseases that may affect judgment or cooperation during the study. Patients with implanted cardiac pacemaker or other electronic implants that may potentially be interfered by the EIT device. Patients with other conditions who are deemed unsuitable for participation by the investigator.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Peking University Third Hospital Beijing China

More Peking University Third Hospital trials in China

Other trials for the same condition

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 NCT07357012 on ClinicalTrials.gov ↗ ← All trials in China