Interactive Design of Patient-Specific Molds for Tissue Shaping
Purpose
The goal of this study is to develop clinical decision-support algorithms for designing participants-specific breast molds for tissue shaping. Autologous breast reconstruction is an important part of breast cancer rehabilitation for many participants. Our goal is to increase the efficiency of autologous breast reconstruction by helping the surgeon design participants-specific molds for shaping tissue into an acceptable breast form.
Condition
- Mastectomy
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Patients 18 years of age or older 2. Patients who are willing and able to provide informed consent 3. Patients who are scheduled to undergo breast reconstruction with free flap (Deep Interior Epigastric Artery Perforator (DIEP) flap or Transverse Rectus Abdominis Myocutaneous (TRAM) flap)
Exclusion Criteria
- Patients whose surgical plan includes the use of stacked flaps (DIEP + other free flap, usually from the thigh or buttock) 2. Patients whose surgical plan includes the use of DIEP flap with vascularized lymph node transfer 3. Patients undergoing neoadjuvant radiation
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover Assignment
- Primary Purpose
- Supportive Care
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Intraoperative Use of 3D Printed Breast Mold |
Participants will be randomized using a 1:1 ration to 1 of 2 conditions |
|
|
Experimental Standard of Care Reconstruction |
Participants will be randomized using a 1:1 ration to 1 of 2 conditions |
|
Recruiting Locations
Houston, Texas 77030
More Details
- NCT ID
- NCT06711965
- Status
- Recruiting
- Sponsor
- M.D. Anderson Cancer Center
Detailed Description
Primary Objective: To evaluate the efficiency of autologous reconstruction performed with 3D-printed participants-specific breast molds designed using our clinical decision-support algorithms. Secondary Objectives: To assess the total number of times the mold was used by the surgeons in the intervention group. To compare the intraoperative time for shaping tissue in control versus intervention group. To collect information on the type of revisions for aesthetic purposes required in control versus intervention group. To assess the number and type of complications experienced in control versus intervention group.