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Completed

NCT Number: NCT00708513

Intraoperative Cell Saver Autotransfusion Use for Major Surgical Oncology Operations.

The purpose of this study is to demonstrate the safety and benefit of auto-transfusion filtered blood in patients undergoing major surgical oncology procedures.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Norton Healthcare, Louisville, Kentucky, United States

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About this study

Homologous blood transfusions during surgical procedures are becoming more challenging, due to lack of adequate reserves and the significant risks of transfusion reactions. Recent advances in the use of patient's own blood (autologous transfusion) has rapidly gained acceptance in major surgical procedures, however due to the requirement for prior planning and the expense of obtaining and storing a patient's blood prior to surgery this alternative is less than ideal.

This research study utilizes a third alternative, a technique called intraoperative autotransfusion, which successfully salvages a patient's blood during surgery and reinfuses the blood back into the patient. The blood salvaging device uses a filtration device that successfully filters out all tumor cells to prevent re-infusion of viable cancer cells.

This study is designed to demonstrate the safety and benefits of the blood salvaging device on patients undergoing major surgical oncology procedures.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Subject is undergoing a major surgical oncology procedure and has potential for extensive blood loss.
  • Subject is ≥ 18 years of age.
  • Subject or Subject's Legally Authorized Representative (LAR) has signed an IRB-approved informed consent form.

Exclusion criteria

  • Subject has medical, social, or psychological factors that, in the opinion of the Investigator, could impact safety or compliance with study procedures.
  • Subject is < 18 years of age.
  • Subject or Subject's LAR did not sign IRB-approved informed consent form.

Treatment and study plan

Primary outcomes

  1. Evaluate the efficacy of intra-operative ultrasound contrast (Definity) administration

    Time frame: Hospital discharge

Sponsors and collaborators

Lead sponsor

University of Louisville

Other

Registry information

Official study title

Phase I/II Evaluation of Intraoperative Autotransfusion Filtration for Major Surgical Oncology Operations

Acronym: Cellsaver

Important dates

Study start
2003
Primary completion
2009
Study completion
2009
First posted
Jul 2, 2008
Registry last updated
Oct 21, 2013

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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