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Clinical Trial Summary

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


Clinical Trial 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


Related Conditions & MeSH terms


NCT number NCT04185961
Study type Interventional
Source Seoul National University Hospital
Contact
Status Completed
Phase N/A
Start date January 6, 2020
Completion date April 6, 2020

See also
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