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Clinical Trial Summary

Since polyacrylamide hydrogel (PAAG) was used in cosmetic surgery in 1997, about 30 million women have received PAAG injection for breast augmentation. Although the use of PAAG has been prohibited in most countries due to its myriad complications, a large number of symptomatic patients and asymptomatic patients have continued to seek medical advice. The strategy of repairing secondary breast deformities after PAAG removal has increasingly become a concern for both doctors and patients, but there is no standardized algorithm yet. The purpose of the present study was to perform a retrospective study to compare the safety and effectiveness of different reconstruction timing and method after removing the gel.


Clinical Trial Description

The primary purposes of this study are to: 1. Compare the safety and effectiveness of IBR vs DBR after PAAG removal; 2. Compare the safety and effectiveness of breast implants with silicone gel prosthesis vs autologous fat transplantation after PAAG removal; 3. Evaluate the clinical characteristics associated with and rates of complications based on reconstruction timing and type. The secondary purposes of this study are toļ¼š 1. Explore and summarize the characteristics of long-term complications of PAAG injection for breast augmentation; 2. Compare the rate of postoperative complications and reoperations between the patients who had breast reconstruction with implants and patients who had primary breast augmentation with implants. 3. Further refine the algorithm for breast reconstruction in patients with PAAG injections. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04715802
Study type Observational
Source First Affiliated Hospital of Zhejiang University
Contact
Status Active, not recruiting
Phase
Start date October 18, 2006
Completion date December 31, 2022

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