膣口のViveve治療の効果を評価する

基本情報

NCT ID: NCT02261974
ステータス: 完了
試験のフェーズ: 該当なし
試験タイプ: 介入
目標被験者数: 186
治験依頼者名: Viveve Inc.

概要

Outside United States (OUS) Post-Market Parallel Group Exploratory Study Design The objective of this study is to determine the safety and effectiveness of the Viveve System to treat the vaginal introitus in women following vaginal birth(s) and in so doing improving vaginal laxity.

対象疾患

Vaginal Laxity Following ChildbirthSexual Function Following Childbirth

介入

Active Treatment Viveve(DEVICE)

Sham Treatment Viveve(DEVICE)

依頼者（Sponsor）

Viveve(INDUSTRY)

実施施設 (2)

Naoe Beauty Clinic

Tokyo, Japan

Yokohama Motomachi Jyosei Iryou Clinic Luna

Kanagawa, Japan