Lymphedema Prevention Through Immediate Lymphatic Reconstruction (LILY) Trial

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

To learn if reconstruction of the lymphatic system at the time of axillary lymphadenectomy can reduce the risk of developing lymphedema.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
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• Participants diagnosed with IBC.

• Participants who have been scheduled for ILR/pLVB by their treating physician/surgeon at the time of their axillary lymphadenectomy for breast cancer

• Participants willing and able to comply with the study protocol requirements and all study-related visit requirements.

• Female subjects at least 18 years old and capable of providing consent to participate.

• Females of childbearing potential must have a negative urine pregnancy test within 36 hours prior to study drug administration and agree to use a medically accepted method of contraception for a period of one month following the study.

Locations
United States
Texas
MD Anderson Cancer Center
RECRUITING
Houston
Contact Information
Primary
Sara Hull, MHA, BA, BSN, RN, CCRP
sehull@mdanderson.org
713-794-1247
Time Frame
Start Date: 2024-09-24
Estimated Completion Date: 2029-08-01
Participants
Target number of participants: 50
Treatments
Experimental: Postoperative Evaluations
Participants who agree to take part in this study, clinic visit timing will be exactly the same time as would ordinarily be scheduled: before surgery, then 6, 12, 18, and 24 months after surgery. Each study visit should take about 2-3 hours.
Related Therapeutic Areas
Sponsors
Leads: M.D. Anderson Cancer Center

This content was sourced from clinicaltrials.gov