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Pathophysiology of urge incontinence in older women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17856439
Enrollment
250
Registered
2006-07-03
Start date
1996-03-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Urge incontinence, detrusor hyperreflexia with impaired contractility (DHIC) Urological and Genital Diseases Urge incontinence

Interventions

1. Immediate release oxybutynin following treatment of reversible causes, dose titrated for four weeks and maintained for further four weeks 2. Control group: placebo

Sponsors

National Institutes of Health (USA)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Cognitively intact, community-dwelling persons at least 55 years old with urge incontinence at least every two days

Exclusion criteria

Exclusion criteria: 1. Significant stress incontinence 2. Outlet obstruction 3. Post-voiding residual (PVR) urine >300 ml 4. Mini mental state examination (MMSE) <24/30 5. Inability to go to the toilet independently 6. Contraindication to antimuscarinic therapy 7. Gastrointestinal obstruction 8. Megacolon 9. Severe liver or renal disease 10. Uncontrolled hyperthyroidism 11. Multiple sclerosis 12. Anteroposterior resection 13. Pelvic radiation 14. Spinal cord disease resulting in para- or quadri-plegia

Design outcomes

Primary

MeasureTime frame
Percentage reduction in incontinence episodes on 4-day bladder diary

Secondary

MeasureTime frame
1. Number of subjects dry at end of study 2. Subjective satisfaction

Countries

United States of America

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026