Breast Reconstruction Clinical Trial
Official title:
Abdominal Scar Improvement in Microsurgical Breast Reconstruction
Microsurgical breast reconstruction is most commonly performed with free abdominal flaps, which leave a long transverse lower abdominal scar. Due to tension across the incision, these scars frequently widen and hypertrophy. Hence, modalities that can reduce this tendency, thus, improving scar appearance are desirable. Here, we wish to investigate the impact of the Neodyne embrace device on postoperative abdominal scar appearance. The proposed study is novel in that it is the first RCT investigating the effect of the embrace device on scar appearance in the context of microsurgical breast reconstruction.
Adult (>18 years) women who have undergone microsurgical breast reconstruction with free abdominal flap(s) approximately 1 week (5-10 days) prior to study participation will be approached by the clinical research team during their first postoperative clinic visit; the protocol asks for the device to be applied at this point. Investigators will only invite those subjects to participate whose incisions, at the 1 week postoperative visit, appear to be uniformly aesthetically similar across the length of the incision. Informed consent for randomization and study participation will be obtained. After eligible patients have provided informed consent, the side of the abdomen to be treated with the Neodyne Device will be randomly selected by opening a sealed randomization envelope. The selected side will be treated with the Neodyne Device through the full study. The Neodyne Device will be applied to a portion of the abdominal incision by the health care provider at 1 week (4-8 days) after the procedure. The other portion of the abdominal incision will serve as the control and will be treated per the investigator's standard of care. Subjects will return to the Investigator's office for a total of 8 weeks for application and removal of the Neodyne Dressing. At the 8th week visit subjects and investigators will complete an evaluation of the incision/scar. Subjects will return to the Investigator's office at 12 weeks from the date of the procedure for another evaluation of the incision/scar. The primary study endpoint will be evaluated at 6 months from the date of the procedure. Subjects will also be offered the opportunity to provide additional photographic evaluations at 12 months after surgery in conjunction with a standard clinic visit. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03757793 -
Near-infrared Spectroscopy for Monitoring Tissue Oxygenation in Breast Reconstruction
|
||
Completed |
NCT05491473 -
Negative Pressure in PAP Donor Sites
|
||
Not yet recruiting |
NCT06013514 -
Post-market Prospective Clinical Study of Nagor Perle Mammary Implants
|
||
Completed |
NCT02169011 -
Secondary Breast Reconstruction With a Flap of Skin From the Back
|
N/A | |
Completed |
NCT01216319 -
Evaluation of the Cook Biodesign Plastic Surgery Matrix
|
N/A | |
Not yet recruiting |
NCT00973544 -
Do Closed Suction Drains Affect the Complications Rate of Breast Reconstruction With Silicone Prosthesis?
|
N/A | |
Completed |
NCT01176786 -
Reusable Versus Disposable Draping System in Breast Reconstruction Surgery
|
N/A | |
Active, not recruiting |
NCT00748722 -
Pre-Operative Imaging of Abdominal Wall Perforators Using CT Angiography
|
N/A | |
Completed |
NCT00753922 -
Core Gel Study of the Safety and Effectiveness of Mentor Round Low Bleed Silicone Gel-filled Mammary Prostheses
|
Phase 3 | |
Completed |
NCT05897463 -
Nipple Neurotization
|
||
Completed |
NCT04350411 -
Comparison of PEAK PlasmaBladeā¢ to Conventional Diathermy in Abdominal Based Free Flap Breast Reconstruction
|
N/A | |
Completed |
NCT06321549 -
New Era of DIEP With Minimally Invasive Mastectomy
|
||
Withdrawn |
NCT03135392 -
Sensation After Nipple Sparing Mastectomy and Breast Reconstruction With or Without Neurotized Free Tissue Transfer
|
N/A | |
Completed |
NCT01256502 -
The SERI® Surgical Scaffold Use in Reconstruction Post Market Study for Tissue Support and Repair in Breast Reconstruction Surgery
|
N/A | |
Active, not recruiting |
NCT04715802 -
Options on the Breast Reconstruction Timing and Method After Removal of Polyacrylamide Hydrogel
|
||
Active, not recruiting |
NCT04491591 -
Implementing BREASTChoice Into Practice
|
N/A | |
Recruiting |
NCT04661501 -
BREAST ADM Trial for Alloplastic Breast Reconstruction
|
N/A | |
Suspended |
NCT03625765 -
Integrated Imaging System for In Vivo Visualization of Free Flap Perfusion Using Indocyanine Dye
|
N/A | |
Withdrawn |
NCT00778947 -
Single Centre Study to Compare Harmonic Scalpel to Conventional Diathermy in Free Tissue Transfer Breast Reconstruction
|
N/A | |
Completed |
NCT00905645 -
Sientra Sponsored Silimed Gel-Filled Breast Implant Core Clinical Study
|
N/A |