Safety And Efficacy Of Solifenacin In Men With Overactive Bladder (OAB) And Detrusor Underactivity

Sponsor
University of L'Aquila (Other)
Overall Status
Completed
CT.gov ID
NCT00441428
Collaborator
(none)
1

Study Details

Study Description

Brief Summary

Detrusor underactivity (DUA) in men is responsible for LUTS in a significant minority, the symptoms being indistinguishable from those seen in BOO. The International Continence Society (ICS) defines DUA as 'a detrusor contraction of inadequate magnitude and/or duration to effect complete bladder emptying in the absence of urethral obstruction. Whilst a reduced maximum urinary flow rate (Qmax) is indicative of voiding dysfunction, flow studies cannot distinguish between DUA and BOO, which are the two principal causes of low flow rates. DUA is diagnosed from a pressure-flow study (PFS)and is characterized by a low-pressure, poorly sustained, or wave-like detrusor contraction with an associated poor flow rate.

Overactive bladder (OAB) is the most common term currently used in clinical medicine to describe a complex of lower urinary tract symptoms (LUTS) with or without incontinence but most commonly consisting of urgency, frequency, nocturia, troublesome or incomplete emptying,and, occasionally, pain. With the exception of pain and incontinence, these symptoms are often found together; thus, the term LUTS has come to replace previous terms, such as urgency-frequency syndrome,urethral syndrome, and prostatism.

Drug treatment is frequently used as the initial management approach for LUTS in older men.Among men who desire treatment, general practice prescribing data have shown that antimuscarinics are not often given to elderly men. There is theoretical concern that the inhibitory effect of antimuscarinics on detrusor contraction could aggravate voiding difficulties or cause urinary retention in patients with BOO. There are virtually no data evaluating the safety and efficacy of solifenacin treatment in men with DUA and OAB.

Condition or Disease Intervention/Treatment Phase

Study Design

Study Type:
Observational
Study Start Date :
Feb 1, 2006
Primary Completion Date :
Jan 1, 2007

Outcome Measures

Primary Outcome Measures

  1. We estimated the safety of solifenacin treatment by measuring the changes to day 120 of voiding function. The following variables were assessed: BVE, BCI, BOOI, Qmax obtained during UDS, PVR []

Secondary Outcome Measures

  1. We estimated the efficacy of solifenacin treatment. For this purpose, the primary efficacy measure was change in the number of urge incontinence episodes per week. Secondary efficacy measures included patient perception of treatment []

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 80 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Men aged > 40 years were eligible if by 7-day bladder diary they had urinary frequency (8 or more micturitions per 24 hours) and urgency, with or without urgency incontinence (1 or more episodes per 24 hours) together with coexistence low detrusor contractility.
Exclusion Criteria:
  • Urinary tract infection,

  • Bladder stone, urogenital tumors,

  • Prostate surgery,

  • Use of indwelling catheter or self-catheterization program,

  • Medications that could affect the lower urinary tract function,

  • History of neurological disease,

  • Acute urinary retention or any condition for which antimuscarinic was contraindicated.

  • Antimuscarinic, antispasmodic, or electrostimulation within 1 month;

  • Any investigational drug within 2 months; or

  • A 5a-reductase inhibitor within 3 months of screening.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of L'Aquila L'Aquila Abruzzo Italy 67100

Sponsors and Collaborators

  • University of L'Aquila

Investigators

  • Principal Investigator: Piero Ronchi, M.D, University of L'Aquila

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00441428
Other Study ID Numbers:
  • UDASOL-1520
First Posted:
Feb 28, 2007
Last Update Posted:
Jun 4, 2008
Last Verified:
Jun 1, 2008

Study Results

No Results Posted as of Jun 4, 2008