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Open Label Phase III Duloxetine Study for Stress Urinary Incontinence

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Lilly

Status and phase

Completed
Phase 3

Conditions

Urinary Incontinence Stress

Treatments

Drug: Duloxetine

Study type

Interventional

Funder types

Industry

Identifiers

NCT00191204
F1J-MC-SBBM
5309

Details and patient eligibility

About

The purpose of this study is to monitor the long term safety of duloxetine in the treatment of stress urinary incontinence.

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female out patients
  • Are ambulatory and are able to use a toilet independently and without difficulty.

Exclusion criteria

  • Use of monoamine oxidase inhibitors (MAOIs)

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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