Cosmesis and quality of life in breast cancer patients undergoing breast conservation therapy
Not Applicable
- Conditions
- Health Condition 1: C50- Malignant neoplasm of breast
- Registration Number
- CTRI/2022/06/043456
- Lead Sponsor
- AIIMS Bhubaneswar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) All patients undergoing breast conservation surgery
2) Female breast cancer (invasive / in situ / sarcoma)
3) Age more than 18 years
4) Patients who are giving informed consent
Exclusion Criteria
1) Patients not eligible for breast conservation surgery
2)Medically unfit for surgery
3) Patients who will not give consent
4) Patient with previous breast surgery
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assess the patient-reported cosmetic outcome of the breast conservation therapy.Timepoint: Pre operative, POD 2, 30 days after surgery, 90 days after surgery, 6 months after surgery
- Secondary Outcome Measures
Name Time Method 1)Assess the objective cosmetic outcome using BCCT.core and three-panel evaluation <br/ ><br>2)Study the factors affecting the cosmetic outcome (Subjective and objective) <br/ ><br>3)Validate English to Odia translation of BREAST-Q Questionnaire and implement the same among survivors of Breast cancer after breast conservation surgery <br/ ><br>4)To study the correlation between subjective and objective methods of outcome and factors influencing discordant results <br/ ><br>5)90 days postoperative morbidity following oncoplastic breast surgery <br/ ><br>6)Mean hospital stay and delay in adjuvant therapy <br/ ><br>7)Mean duration of treatment completion post oncoplastic breast surgery <br/ ><br>Timepoint: Pre operative, POD 2, 30 days after surgery, 90 days after surgery, 6 months after surgery