Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:41 PM
Ignite Modification Date:
2025-12-24 @ 4:41 PM
NCT ID:
NCT01366066
Eligibility Criteria:
Inclusion Criteria:
* Women suffering from stress incontinence OR Women suffering from urge incontinence /overactive bladder syndrome
* Ongoing anticholinergic treatment in the urge incontinence/overactive bladder syndrome group
* Patient capable of understanding protocol and performing treatment
Exclusion Criteria:
* On going pregnancy or breast feeding
* Treatment with anticholinergic medications in the stress incontinence group
* Treatment with diuretic drugs
* Acute illness (including infection, trauma and haematuria)
* Fibromyalgia
* Faecal incontinence
* Known neurological disease
* Bladder pain syndrome
* Genital prolaps \> stage 2 on the Pelvic Organ Prolapse Quantification System POP-Q
* Previous treatment with neuromodulation or Botox
* Previous pelvic floor surgery or radiation
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT01366066
Study Brief:
Protocol Section:
NCT01366066