Viewing Study NCT06258863



Ignite Creation Date: 2024-05-06 @ 8:05 PM
Last Modification Date: 2024-10-26 @ 3:20 PM
Study NCT ID: NCT06258863
Status: ENROLLING_BY_INVITATION
Last Update Posted: 2024-02-14
First Post: 2024-01-15

Brief Title: Investigating the Effects of Different Incision Types on Aesthetic Outcomes and Incision-related Complications After Breast Reconstruction Surgery
Sponsor: Hubei Cancer Hospital
Organization: Hubei Cancer Hospital

Study Overview

Official Title: Investigating the Effects of Different Incision Types on Aesthetic Outcomes and Incision-related Complications After Breast Reconstruction Surgery
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2023-11
Last Known Status: None
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: None
Brief Summary: 1 DATA COLLECTION About 300 cases of female patients who underwent breast reconstruction at Hubei Cancer HospitalHBCH between February 2013 and June 2023 were retrospectively collected The incision was defined as the mastectomy incision and was grouped by the commonly used inframammary fold incision lateral chest wall incision circumareolar incision and radial incision The incidence of postoperative incision-related complications was recorded for different incision types
2 DATA ORGANIZATION Patients were divided into subgroups based on history of previous breast surgery location and size of the lump retention of the nipple-areola complex timing of reconstruction and type of the implant The correlation of each subgroup with incision design is discussed
3 FOLLOW-UP Collected cases were followed up by telephone to complete the Breast-Q questionnaire aesthetic score
4 DATA ANALYSIS The incidence of postoperative incision-related complications and aesthetic scores for different incision types were statistically analyzed
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None