Observation of surgical related Cosmesis and Cosmesis related outcome reported by patients after patient’s breast conservation surgery and reconstructio
Not Applicable
- Conditions
- Health Condition 1: C509- Malignant neoplasm of breast of unspecified site
- Registration Number
- CTRI/2024/05/066667
- Lead Sponsor
- Tata Memorial Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.All patients who have undergone a breast conservative surgery (from Jun 2014 to June 2023) with a Transposition Flap
2.All patients willing for the study
Exclusion Criteria
1.All patients undergoing procedures other than Transposition Flap.
2.All metastatic patients.
3.Patients not willing to give consent.
4.Pregnant women
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient reported outcome measure obtained by the BREAST-Q BCS module. <br/ ><br>Timepoint: the patients will be administered the BREAST-Q BCS module at Baseline visit
- Secondary Outcome Measures
Name Time Method 1.Clinical outcome parameters such as margin positive rate, local recurrence and disease-free survival. <br/ ><br>2.Subjective cosmetic assessment by Modified Harvard Scale5 <br/ ><br>3.Objective cosmetic assessment by BCCT.Core software <br/ ><br>Timepoint: at baseline visit