Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05363189

Optimizing Postoperative Recovery After Breast Reconstruction With Autologous Tissue (BestDIEP)

Status
Recruiting
Phase
Study type
Observational
Enrollment
380 (estimated)
Sponsor
Vastra Gotaland Region · Other Government
Sex
Female
Age
18 Years – 100 Years
Healthy volunteers
Not accepted

Summary

Women who have their breast reconstructed with autologous tissue seem to be more satisfied with their breast. However, autologous breast reconstruction entails a bigger operation, and the usage of more health care resources, than some other methods, such as implant-based techniques. The main objectives of the present study are to investigate if pre- peri- and postoperative protocols can be safely modified, so the operation demands less resources, while maintaining a low complication rate and a high patient satisfaction.

Conditions

Interventions

TypeNameDescription
PROCEDUREVenous augmentationIncreasing the venous drainage of a deep inferior epigastric artery perforator (DIEP) flap by anastomosing the superficial inferior epigastric vein to the cephalic vein
PROCEDURETraditional ERAS (enhanced recovery after surgery) protocolPre-, peri-, and post-operative care as described in the ERAS protocol
PROCEDURESahlgrenska recovery protocolPre-, peri-, and post-operative care as described in the Sahlgrenska recovery protocol
PROCEDURENo venous augmentationTraditional deep inferior epigastric artery perforator flap (DIEP)

Timeline

Start date
2022-05-02
Primary completion
2026-12-31
Completion
2026-12-31
First posted
2022-05-05
Last updated
2025-07-03

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT05363189. Inclusion in this directory is not an endorsement.