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Evaluation of Efficacy and Safety of Votiva for Vaginal Rejuvenation

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03520426
Recruitment Status : Unknown
Verified April 2018 by Jennifer Walden, Walden, Jennifer L., M.D.,P.L.L.C..
Recruitment status was:  Recruiting
First Posted : May 9, 2018
Last Update Posted : May 9, 2018
Sponsor:
Collaborators:
Aviva Preminger, MD., P.L.L.C.
InMode MD Ltd.
Information provided by (Responsible Party):
Jennifer Walden, Walden, Jennifer L., M.D.,P.L.L.C.

No Study Results Posted on ClinicalTrials.gov for this Study
Recruitment Status : Unknown
Estimated Primary Completion Date : January 30, 2020
Estimated Study Completion Date : January 30, 2020
Publications:
Coad JE, Vos JA, Curtis A, Krychman M. Safety and mechanisms of action supporting nonablative radiofrequency thermal therapy for vaginal introitus laxity occurring in women after childbirth: Histological study in the sheep vaginal model. J Sex Med 2013;10(Supplement 2):175.