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Study identifier: NCT04772131 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Desara ® One Single Incision Sling 522 Study

Condition: Stress Urinary Incontinence  ·  Sponsor: Caldera Medical, Inc.

PhaseNA
Planned participants300
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

A post-market study to compare the safety and effectiveness of the Desara® One Single Incision Sling (SIS), when compared to that of an FDA cleared transobturator sling over a period of 36 months.

This description comes directly from the study's public registry record.

Talk to the study team

Vicki Gail  ·  818-483-7602  ·  vgail@calderamedical.com

Always discuss trial participation with your own doctor first.

Locations (15)

Valley Urogynecology Associates, Inc.Phoenix, Arizona, United StatesRecruiting
University of Arizona College of MedicineTucson, Arizona, United StatesNot Yet Recruiting
Urological Research Center CorpHialeah, Florida, United StatesRecruiting
Women's Health Care Associates P.A. dba Rosemark Women Care SpecialistsIdaho Falls, Idaho, United StatesRecruiting
CMB Research, LLCNewburgh, Indiana, United StatesRecruiting
University of LouisvilleLouisville, Kentucky, United StatesRecruiting
Mt. Auburn Hospital Division of UrogynecologyCambridge, Massachusetts, United StatesRecruiting
Specialty Clinical Research of St. Louis, LLCSt Louis, Missouri, United StatesRecruiting
Women's Cancer Center of NevadaLas Vegas, Nevada, United StatesRecruiting
University of New MexicoAlbuquerque, New Mexico, United StatesRecruiting
Novant Health UrogynecologyCharlotte, North Carolina, United StatesRecruiting
The Lindner Research Center at The Christ HospitalCincinnati, Ohio, United StatesRecruiting

+ 3 more locations — full list on the registry record.

Follow this study

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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT04772131