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An 8 Week Study Looking At The Efficacy, Toleration And Safety Of SS-RBX For Stress Urinary Incontinence.

Pfizer logo

Pfizer

Status and phase

Completed
Phase 2

Conditions

Urinary Incontinence, Stress

Treatments

Drug: SS-RBX

Study type

Interventional

Funder types

Industry

Identifiers

NCT00138749
A6061023

Details and patient eligibility

About

A study designed to assess the efficacy, toleration and safety of SS-RBX for the treatment of stress urinary incontinence.

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Clinically significant stress urinary incontinence

Exclusion criteria

  • History or evidence of any relevant confounding urological or neurological disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

95

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Data sourced from clinicaltrials.gov

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