Clinical Trials Directory

Trials / Completed

CompletedNCT01705444

The Spanner Prostatic Stent and Patient's Quality of Life

The Impact of the Temporary Stent on Parameters of Voiding Function and on the Quality of Life Among Patients With LUTS

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
88 (actual)
Sponsor
Princess Al-Johara Al-Ibrahim Cancer Research Center · Academic / Other
Sex
Male
Age
45 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Acute urinary retention is considered one of the most common problems in the older age, especially those who have benign prostatic hyperplasia. Solving the problem of acute urinary retention using the Foley catheter still causes problems at the level of patient movement and the daily exercises. However, with the emergence of a new device, the spanner, investigators believe that many of the above mentioned problems can be resolved. This tool may provide more freedom for the patient.

Detailed description

This research comes up to date with technological innovations in the field of health where investigators want to evaluate the efficacy of a new catheter (The Spanner) to reduce the acute urinary retention and to determine whether they are consistent with the daily life of the patient, compared to the Foley catheter previously used. The study include all patients with acute urinary retention due to prostatic obstruction. Subjects were excluded if they had prior surgery for prostate cancer, had any other urethral or bladder surgery, or if they were at high risk of developing bladder or kidney stones The study will be national community based study conducted in different hospitals in Saudi Arabia. Investigators will test two different types of stents in patients with acute urinary retention for a short period (not exceeding five days), find out the compatibility of these stents with the daily life of the patient and determine their impact on his quality of life using an appropriate questionnaire after each use.

Conditions

Interventions

TypeNameDescription
DEVICEFoley Catheter and The Spanner InsertionA Foley catheter will be inserted for 3-5 days, then a voiding trail will be attempted by the patient himself without the catheter. Then, the Spanner will be inserted into the same patient for another 3-5 days and an evacuation trail will be attempted also by the patient after removal of the Spanner. Treatment Satisfaction Questionnaire (TSQ) will be applied by the same person to the patient twice, once after removal of the Foley catheter and the second after removal of the Spanner.

Timeline

Start date
2012-03-01
Primary completion
2016-03-01
Completion
2016-03-01
First posted
2012-10-12
Last updated
2016-03-31

Locations

1 site across 1 country: Saudi Arabia

Source: ClinicalTrials.gov record NCT01705444. Inclusion in this directory is not an endorsement.