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OpenTrials
Completed

NCT Number: NCT00543764

Intraoperative Pathway in DIEP Flap Breast Reconstruction

Efficiency in the operating room can be difficult in long cases with multiple surgeons. We used a team based approach to develop an intraoperative pathway for microsurgical breast reconstruction with a deep inferior epigastric perforator flap.

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Key information

Sex eligibility

Female

Study type

Observational

Primary location

Beth Israel Deaconess Medical Center

Boston, Massachusetts, 02215, United States

About this study

A team based approach was developed with an intraoperative pathway for microsurgical breast reconstruction with a deep inferior epigastric perforator flap.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All cases prior to pathway

Exclusion criteria

  • None

Treatment and study plan

Pathway

Other

Comparison of pre and post pathway

Other names: intraoperative pathway

Primary outcomes

  1. Operative Time

    Time frame: 3 years

    Length of Time in surgery

Sponsors and collaborators

Lead sponsor

Beth Israel Deaconess Medical Center

Other

Registry information

Important dates

Study start
2005
Primary completion
2008
Study completion
2011
First posted
Oct 15, 2007
Registry last updated
Mar 7, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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