CompletedNCT07413692
BTL-699-2 and HPM-6000UF Devices for the Improvement of Depressive Symptoms and Urinary Incontinence in Postpartum and Early Post-Childbirth Women
Device studyAges 22–60United StatesDepression
Understand this study
Who was this study for?
Listed age limits: 22 years to 60 years.
- Listed locations
- Garfield Heights and 2 more locationsSee all locations and recruitment
Study information
Study start dateStarted: November 25, 2025
- Recruitment status
- Completed
- Enrollment listed in the registry
- 30
- Sponsor
- BTL Industries Ltd.
- Sponsor type
- Other organization
- Study type
- Device
- Intervention type
- DEVICE
- Study phase
- Not clearly listed
- Locations
- United States
- Age range
- From 22 Years to 60 Years
- Official registry ID
- NCT07413692
- Official title
Show the full official title
Safety and Efficacy of the Combined BTL-699-2 and HPM-6000UF Devices for the Improvement of Depressive Symptoms and Urinary Incontinence Among Postpartum Women and Women up to Five Years After Childbirth
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Explore recruiting studiesRecruitment & locations
CompletedThis badge reflects the study status reported by the registry. Check the registry for the latest information.
Garfield Heights · Oklahoma City · Dallas
Questions about this study
Who is behind this study?
The study sponsor is BTL Industries Ltd.
Who was this study for?
Listed age limits: 22 years to 60 years.
