Patient Reported Outcome Measures (PROMs) in breast reconstruction: a prospective cohort study.

Withdrawn

• Conditions: breast reconstruction; mamma reconstruction; 10006291

• Registration Number: NL-OMON40835
• Lead Sponsor: HagaZiekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Withdrawn
• Sex: Not specified
• Target Recruitment: 260

Inclusion Criteria

Women in need of a mastectomy or who had a mastectomy in the past and eligible for a breast reconstruction.

Exclusion Criteria

Women who are not able to speek Dutch

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The differences in pre- and postoperative scores of well-being and satisfaction<br /><br>of the patient's. This will be scored by the use of the Breast-Q questionnaire.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Differences in pre- and postoperative scores, compared wtih the different<br /><br>surgical techniques:<br /><br>- DIEP-method<br /><br>- LD-method<br /><br>- LD-method with tissue expander/protheses<br /><br>- Prothese<br /><br>- Tissue expander with prothese</p><br>