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Completed

NCT Number: NCT01315119

SPY Intra-Operative Angiography & Skin Perfusion in Immediate Breast Reconstruction w/ Implants

The investigators hope to learn the value of the SPY ELITE® intra-operative angiography in reducing post-operative complications associated with low breast skin blood flow after breast reconstruction using implants.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Stanford University School of Medicine

Stanford, California, 94305, United States

About this study

Breast cancer is the most common malignancy among women, and over 180,000 women will be diagnosed with this disease in 2008. Last year, over 57,000 breast reconstructive procedures were performed, of which prosthetic reconstruction constituted 76%. Immediate reconstruction has been favored over delayed procedures for psychological and technical reasons. However, immediate breast reconstruction is associated with significantly higher complication rates (50-52%) than delayed procedures (32-36%), especially when a prosthetic technique is used. For prosthetic reconstructions, the most significant early complications include necrosis of the mastectomy skin flaps, infection, delayed wound healing and exposure of the implant. The published incidence of these complications ranges between 10% and 40% and is predominantly associated with malperfusion of mastectomy skin flaps. Thus, evaluation of skin perfusion and elimination of poorly vascularized areas could help reduce the high rate of complications in immediate breast reconstruction.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

3.1.0 Ability to understand and the willingness to sign a written informed consent document.

3.1.1 Signed written informed consent.

3.1.2 Women with local or regional recurrences after previous breast conserving surgery.

3.1.3 Women undergoing delayed post mastectomy reconstruction.

3.1.4 Women undergoing prophylactic mastectomy.

3.1.5 Women with invasive or non-invasive breast cancer, receiving breast conserving surgery with or without reduction mammoplasty or mastectomy, with or without immediate reconstruction.

3.1.6 Women of 18 years of age or older.

3.1.7 ECOG or Karnofsky Performance Status 0,1,2.

3.1.8 Basic Metabolic Panel within 6 months

3.1.9 Psychiatric or addictive disorders or other conditions that, in the opinion of the investigator, would preclude the patient from meeting the study requirements.

Exclusion criteria

3.2.1 History of liver or kidney failure will not be eligible.

3.2.2 Allergies to iodine containing products will not be eligible.

3.2.3 Women who are pregnant will not be eligible.

Treatment and study plan

SPY Intra-Operative Angiography

Procedure

Calculated per patient

Other names: Novadaq SPY

Primary outcomes

  1. To compare clinical visual assessment of skin viability with intraoperative SPY imaging.

    Time frame: During surgery

  2. To compare clinical visual assessment of skin viability with intraoperative SPY imaging.

    Time frame: Immediately post operative

  3. To compare clinical visual assessment of skin viability with intraoperative SPY imaging.

    Time frame: 2 weeks

  4. To compare clinical visual assessment of skin viability with intraoperative SPY imaging.

    Time frame: 1 month

  5. To compare clinical visual assessment of skin viability with intraoperative SPY imaging.

    Time frame: 3 months

  6. To compare clinical visual assessment of skin viability with intraoperative SPY imaging.

    Time frame: 6 months

  7. To compare clinical visual assessment of skin viability with intraoperative SPY imaging.

    Time frame: 12 months

Secondary outcomes

  1. Establish the percentage of patients with ischemia or necrosis in the first year post surgery.

    Time frame: 12 months

  2. Number and type of complications in the first year.

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Registry information

Official study title

The Role of SPY Intra-Operative Angiography in Determining Adequate Skin Perfusion in Immediate Breast Reconstruction With Implants

Important dates

Study start
2011
Primary completion
2014
Study completion
2015
First posted
Mar 15, 2011
Registry last updated
Aug 6, 2021

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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