Skip to content

Management of the Idiopathic Overactive Bladder With Botulinum Toxin: Systematic Review

Management of the Idiopathic Overactive Bladder With Intradetrusor Injection of Type-A Botulinum Toxin: Systematic Review of the Literature

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01750645
Enrollment
Unknown
Registered
2012-12-17
Start date
2012-07-31
Completion date
2013-01-31
Last updated
2012-12-17

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

Conditions

Urinary Bladder, Overactive

Brief summary

Overactive bladder is defined as a syndrome composed of urgency, increased urinary frequency, and sometimes urinary incontinence; its etiology may be characterized as neurogenic or non-neurogenic (i.e., idiopathic). This illness has a great impact in quality of life and one of the available treatments is the injection of Botulinum Toxin. This study aims to review the efficacy and safety of type-A Botulinum Toxin in the management of Idiopathic Overactive Bladder. A systematic search was performed in MEDLINE, EMBASE, CENTRAL and LILACS, and the controlled randomized clinical trials were chosen to review with the CONSORT criteria by independent reviewers. Outcomes analyzed were the efficacy of the intervention for relieving the symptoms (urgency, frequency and urgency incontinence), adverse events to treatment, change in quality of life and urodynamic measures.

Interventions

DRUGIntradetrusor Injection of Type-A Botulinum Toxin
OTHEROther interventions analyzed according to protocol

* Placebo * Different dosage of Type-A Botulinum Toxin injected * Anticholinergic drugs

Sponsors

Clínica Infantil Colsubsidio
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Controlled randomized clinical trials * Adult patients diagnosed with idiopathic overactive bladder * Language of the study: english

Exclusion criteria

* Diagnosis of neurogenic overactive bladder * Patients under 18 years old * Use of Type-B Botulinum Toxin as the intervention * Other types of studies

Design outcomes

Primary

MeasureTime frame
Efficacy of the intervention for relieving the symptoms (urgency, frequency and urgency incontinence)Minimun follow-up period of 12 weeks

Secondary

MeasureTime frameDescription
Adverse events to treatment (urinary retention and urinary tract infections)Minimun follow-up period of 12 weeks
Change in quality of lifeMinimun follow-up period of 12 weeks
Change in urodynamic measuresMinimun follow-up period of 12 weeksIncrease in maximum cystometric capacity, first desire to void, normal desire to void, postvoid residual volume, and the presence/abscence of detrusor overactivity.

Countries

Colombia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026