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Standardization for reliable uroflowmetry testing

Standardization for reliable uroflowmetry testing - Standardization for reliable uroflowmetry testing

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000035446
Enrollment
150
Registered
2019-01-21
Start date
2019-01-04
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prospective

Interventions

Control group&#39
s uroflowmetry after drinking 1500 ml water Control group&#39
s uroflowmetry when the volunteer has full blader Benign prostatic hyperplasia patient&#39
group uroflowmetry after drinking 1500 ml water Benign prostatic hyperplasia patient&#39
group uroflowmetry when the patient has full blader

Sponsors

Erman Ceyhan, M.D. Idil State Hospital
Lead Sponsor
Mehmet Kazim Asutay, M.D.
Collaborator

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: - Having benign prostatic hyperplasia in patient group - Healty volunteers whom have no lower urinary tract symptoms - Participants able to void into uroflowmetry container spontainously - Participants over 30 years old

Exclusion criteria

Exclusion criteria: - patients suffering neurological disorders - patients suffering over-active bladder - patients with urinary incontinence

Design outcomes

Primary

MeasureTime frame
To attain a voided volume over 150 ml in a uroflowmetry test after drinking 1500 ml of water in one hour.

Secondary

MeasureTime frame
-Promoting premedicated uroflowmetry testing as suboptimal test results are likely othervise -Assessing whether the suboptimal uroflowmetry results is patient related or hydration related

Countries

Europe

Contacts

Public ContactErman Ceyhan

Idil State Hospital Urology Clinic

erman_ceyhan@yahoo.com00905355873688

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026