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Study identifier: NCT06290193 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of Acute Normovolemic Hemodilution (ANH) in People With Ovarian Cancer Who Are Having Cytoreductive Surgery

Condition: Ovarian Cancer · Fallopian Tube Carcinoma · Ovarian Carcinoma  ·  Sponsor: Memorial Sloan Kettering Cancer Center

PhasePhase 2
Planned participants86
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Participants will be scheduled for primary cytoreductive surgery as part of their standard care. Before surgery, participants will be assigned by chance to a study group. Depending on which group they are in, they will receive either acute normovolemic hemodilution/ANH during surgery or standard surgical management during surgery. The researchers think acute normovolemic hemodilution/ANH may decrease the need for allogenic blood transfusion/ABT in people having primary cytoreductive surgery.

This description comes directly from the study's public registry record.

Talk to the study team

Dennis Chi, MD  ·  212-639-5016  ·  chid@mskcc.org

Ginger Gardner, MD  ·  212-639-2375  ·  gardnerg@mskcc.org

Always discuss trial participation with your own doctor first.

Locations (7)

Memoral Sloan Kettering at Basking Ridge (Limited Protocol Activities)Basking Ridge, New Jersey, United StatesRecruiting
Memorial Sloan Kettering Monmouth (Limited protocol activities)Middletown, New Jersey, United StatesRecruiting
Memorial Sloan Kettering Bergen (Limited protocol activities)Montvale, New Jersey, United StatesRecruiting
Memorial Sloan Kettering Cancer Center @ Suffolk-Commack (Limited protocol activities)Commack, New York, United StatesRecruiting
Memorial Sloan Kettering Westchester (Limited protocol activities)Harrison, New York, United StatesRecruiting
Memorial Sloan Kettering Cancer Center (All protocol activities)New York, New York, United StatesRecruiting
Memorial Sloan Kettering Nassau (Limited Protocol Activities)Uniondale, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06290193