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Pilot Study to Determine the Optimal Negative Pressure for Non-invasive Breast Augmentation in Women

2019-12-10 01:21:01 | BioPortfolio

Summary

Aim is to investigate optimum pressure and evaluate safety and effectiveness of EVERA-RAPHA for breast augmentation

Description

1. Subjects who voluntarily signed a consent form and met all inclusion / exclusion criteria should enroll in this study.

2. Subjects enrolled in the study will be randomized and assigned to either Group1 or Group2 in a 1: 1 ratio.

3. Apply EVERA RAPHA for 4 weeks

3. Measure breast circumference and breast volume at Baseline and 4weeks later 4. Visit after 4 weeks to evaluate safety and effectiveness

Study Design

Conditions

Breast Hypoplasia

Intervention

EVERA-RAPHA with 60mmHG, EVERA-RAPHA with 100mmHG

Status

Not yet recruiting

Source

Seoul National University Hospital

Results (where available)

View Results

Links

Published on BioPortfolio: 2019-12-10T01:21:01-0500

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Medical and Biotech [MESH] Definitions

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