A longitudinal non-invasive study of changes in urinary bladder contractility secondary to benign prostatic hyperplasia.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON29657

Enrollment

1020

Registered

2005-09-09

Start date

2001-11-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Benign prostatic hyperplasia (BPH)

Interventions

Non-invasive measurement of the urinary bladder pressure.

Eligibility

Inclusion criteria

Inclusion criteria: 1. Men aged 38-77; 2. Mentally and physically able to complete a voiding diary and to visit the outpatient clinic; 3. Written informed consent to participate in the trial.

Exclusion criteria

Exclusion criteria: 1. Unable to urinate in a standing position; 2. Previous lower urinary tract surgery; 3. Congenital disease of the lower urinary tract; 4. Use of medication or other interventions for lower urinary tract symptoms; 5. Other diseases that could alter urinary function (e.g. Parkinson, CVA, DM, kidney failure, bladder/prostate cancer, current urinary tract infection); 6. Heart failure; 7. Voiding pattern at first visit incompatible with measurement technique, e.g. flow rate too low (<6 ml/s), interrupted voiding, straining; 8. Mentally or physically unable to complete a voiding diary and to visit the outpatient clinic; 9. Use anticoagulants.

Design outcomes

Primary

Measure	Time frame
The study is observational, there is no endpoint.	—

Contacts

Public ContactR. Mastrigt, van

Erasmus Medical Center, Josephine Nefkens Institute, Department of Urology, Urodynamics, P.O. Box 1738

r.vanmastrigt@erasmusmc.nl+31 (0)10 4088058

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)