Clinical trial · Observational
Optimizing Postoperative Recovery After Breast Reconstruction With Autologous Tissue (BestDIEP)
NCT05363189CI-TRIAL-00091722BestDIEPrecruitingClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Breast Reconstruction | — | UNRESOLVED | — |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| No venous augmentation | Procedure | — | UNRESOLVED |
| Sahlgrenska recovery protocol | Procedure | — | UNRESOLVED |
| Traditional ERAS (enhanced recovery after surgery) protocol | Procedure | — | UNRESOLVED |
| Venous augmentation | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- label
- No venons augmentation
- description
- Retrospective group of patients who have not received venous augmentation during their operation.
- interventionNames
- Procedure: No venous augmentation
- label
- Venous augmentation
- description
- Retrospective group of patients who have received venous augmentation during their operation.
- interventionNames
- Procedure: Venous augmentation
- label
- ERAS protocol
- description
- Retrospective group operated according to the traditional ERAS (enhanced recovery after surgery) protocol
- interventionNames
- Procedure: Traditional ERAS (enhanced recovery after surgery) protocol
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 100 Years
Show eligibility criteria text
Inclusion Criteria: * Operated or will be operated with a DIEP flap in the department * \>18 years of age Exclusion Criteria: * Inability to leave informed consent * Inability to understand and speak Swedish (for the questionnaire)
References
Publications (0)
Data not yet available
No reference posted for this study.