Efficacy of Conservative Treatments for Urinary Incontinence in Women

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age20-100
SponsorMackay Medical College

About this trial

To conduct a retrospective study to examine the effect of these conservative treatments to the symptoms and quality of life of patients with urinary incontinence. The investigators will use both subjective and objective assessment parameters, such as self-report symptoms, bladder diary, pad test and urodynamic study to access the improvement.

Eligibility criteria

Qualifiers

Adult female patient diagnosed with urinary incontinence through clinical assessment

Diagnosed at Mackay Memorial Hospital and underwent non-surgical treatment and subsequent follow-up.

Disqualifiers

Choosing invasive or surgical treatment options (such as bladder botulinum toxin injection, urethral sling surgery).

Unable to comply with regular follow-up for at least one year.

Pregnant women

Patients with a history of neuromuscular disorders.

Trial design

Treatments tested in this trial

  • BT
  • bPFMT
  • iVES
  • BT + bPFMT
  • BT + iVES
  • bPFMT + iVES

Treatment groups

60 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.

Sponsors and collaborators