Evaluating quality of life after oncoplastic surgery for breast cancer
IRONY: lIfe afteR ONcoplastic surgerY
This study tests how oncoplastic surgery affects the quality of life for breast cancer patients by looking at their recovery and satisfaction after the procedure.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 250 (estimated) |
| Ages | 18 Years to 85 Years |
| Sex | Female |
| Sponsor | Campus Bio-Medico University Academic / other |
| Locations | 1 site (Roma) |
| Trial ID | NCT05842148 on ClinicalTrials.gov |
What this trial studies
This study evaluates the quality of life in breast cancer patients who undergo conservative oncoplastic surgery. It focuses on assessing oncological, aesthetic, and functional outcomes in a prospective sample of 250 patients using unilateral or bilateral remodeling techniques. Data will be collected on post-surgical complications and patient-reported outcomes through questionnaires, alongside histopathological evaluations. The aim is to understand the impact of surgical techniques on patients' overall well-being and recovery.
Who should consider this trial
Good fit: Ideal candidates are breast cancer patients eligible for conservative oncoplastic surgery who can provide informed consent.
Not a fit: Patients who are pregnant, breastfeeding, or in emergency situations may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the understanding of how oncoplastic surgery affects the quality of life for breast cancer patients.
How similar studies have performed: Other studies have shown promising results in evaluating quality of life after similar surgical approaches, indicating potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Clinical diagnosis of breast cancer * Must be able for conservative oncoplastic surgery with type 1 and 2 procedures who give informed consent to the study. Exclusion Criteria: * Patients who are pregnant or breastfeeding * Patients in emergency situations * Subjects unable to understand and want
Where this trial is running
Roma
- Paolo Orsaria, MD. PhD; [porsaria] — Roma, Italy (Recruiting)
Study contacts
- Principal investigator: Paolo Orsaria, Surgeon; — Policlinico Universitario Campus Bio-Medico
- Study coordinator: Paolo Orsaria, MD, PhD;
- Email: p.orsaria@policlinicocampus.it
- Phone: 3282492485
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.