Improving recovery after breast reconstruction using autologous tissue

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates how to optimize postoperative recovery for women undergoing breast reconstruction with autologous tissue, specifically the DIEP flap technique. It aims to modify pre-, peri-, and postoperative protocols to reduce healthcare resource usage while ensuring low complication rates and high patient satisfaction. The study will evaluate various interventions, including venous augmentation and enhanced recovery after surgery (ERAS) protocols, to determine their effectiveness in improving recovery outcomes.

Why it matters

Who can join: the full rules

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)

Where it's running

• Sahlgrenska university hospital
  Gothenburg, Sweden Recruiting

Study contacts

• Study coordinator: Emma Hansson, MD, PhD
• Email: emma.em.hansson@vgregion.se
• Phone: 0046313421000

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.