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A Study of a Comprehensive Prevention Program to Reduce Lymphedema After Axillary Lymph Node Dissection in People With Breast Cancer

RECRUITINGPhase 3Sponsored by Memorial Sloan Kettering Cancer Center
Actively Recruiting
PhasePhase 3
SponsorMemorial Sloan Kettering Cancer Center
Started2023-11-16
Est. completion2030-03-16
Eligibility
Age18 Years – 75 Years
SexFEMALE
Healthy vol.Accepted
Locations7 sites
View on ClinicalTrials.gov →

NCT06144164

Summary

The purpose of this study to test whether a comprehensive program may help the lymph fluid to drain out of the arm and prevent lymphedema in participants with breast cancer.

Eligibility

Age: 18 Years – 75 YearsSex: FEMALEHealthy volunteers accepted
Inclusion Criteria:

* Female sex
* Diagnosis of breast cancer
* Ages 18 to 75 years
* Consented for unilateral ALND or for unilateral SLNB with possible ALND

Exclusion Criteria:

* Male sex
* Does not speak English
* Does not fit into study garment
* Axillary recurrence
* History of ALND
* Requirement of bilateral ALND for the treatment of breast cancer
* Treatment with SLNB only
* Known anaphylactic allergy to ICG dye used in ILR
* Impaired decision-making capacity

Conditions7

Breast CancerBreast CarcinomaCancerFemale Breast CancerLymphedemaLymphedema ArmLymphedema of Upper Arm

Locations7 sites

Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities)
Basking Ridge, New Jersey, 07920
Michelle Coriddi, MD646-608-8042
Memorial Sloan Kettering Monmouth (Limited Protocol Activities)
Middletown, New Jersey, 07748
Michelle Coriddi, MD646-608-8042
Memorial Sloan Kettering Bergen (Limited Protocol Activities)
Montvale, New Jersey, 07645
Michelle Coriddi, MD646-608-8042
Memorial Sloan Kettering Commack (Limited Protocol Activities)
Commack, New York, 11725
Michelle Coriddi, MD646-608-8042
Memorial Sloan Kettering Westchester (Limited Protocol Activities)
Harrison, New York, 10604
Michelle Coriddi, MD646-608-8042

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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