Host Response to Pessaries in Microbial Communities of the Postmenopausal Vagina
Completed
Conditions studied: Stress Urinary Incontinence, Prolapse
In brief
The ability to determine the postmenopausal vaginal environment and the impact of pessary use could help to maximize pessary therapy and non-surgical treatment for such a prevalent problem.
Key facts
- Study ID
- NCT02605135
- Run by
- Loyola University
- People needed
- 84
- Starts
- 2016-04-01
- Expected to finish
- 2018-06-01
- Last updated by the study team
- 2019-01-22
Who can join
Age: 51 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- must be English speaking
- appropriate for pessary treatment
- pelvic floor conditions such as POP (with or without the presence of a uterus), stress urinary incontinence, urge urinary incontinence, or any combination of the above.
You may not qualify if…
- a history of current, symptomatic vaginal stricture
- a history of current, radiation therapy,
- or current treatment with auto-immune suppression agents.
- if they have eroded mesh in the vagina from prior pelvic floor surgery
Where it is running
- Loyola University Medical Center — Maywood, Illinois, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.