Ignite Creation Date:
2025-12-18 @ 10:05 AM
Ignite Modification Date:
2025-12-23 @ 10:14 PM
Study NCT ID:
NCT00748722
Status:
None
Last Update Posted:
2008-09-09 00:00:00
First Post:
2008-07-15 00:00:00
Is Possible Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Pre-Operative Imaging of Abdominal Wall Perforators Using CT Angiography
Sponsor:
None
Organization:
Study Overview
Official Title:
Pre-Operative Imaging of Abdominal Wall Perforators Using CT Angiography for DIEP Breast Reconstruction
Status:
None
Status Verified Date:
2008-09
Last Known Status:
ACTIVE_NOT_RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
DIEP
Brief Summary:
Abdominal donor-site flaps, including the transverse rectus abdominis musculocutaneous (TRAM) and deep inferior epigastric artery perforator flaps(DIEP), are standard in autologous breast reconstruction. With significant variation in the vascular anatomy of the abdominal wall, preoperative imaging is essential for preoperative planning and reducing intraoperative error.
The quest continues for optimal preoperative assessment. Computed tomographic angiography has recently been proposed as a noninvasive modality for this purpose. It provides the location of the perforator vessels, diameter and anatomic course in regards to the rectus muscle.
In this study we will perform preoperative lower abdominal computed tomographic angiography in DIEP flap breast reconstruction patients.
We plan to study 20 patients, eligible for lower abdominal-based breast reconstruction.
The quest continues for optimal preoperative assessment. Computed tomographic angiography has recently been proposed as a noninvasive modality for this purpose. It provides the location of the perforator vessels, diameter and anatomic course in regards to the rectus muscle.
In this study we will perform preoperative lower abdominal computed tomographic angiography in DIEP flap breast reconstruction patients.
We plan to study 20 patients, eligible for lower abdominal-based breast reconstruction.
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: