Clin2
NCT04722692Possibly a fitRecruiting

Delayed sentinel lymph node biopsy for ductal cancer in situ

DCISBreast CancerBreast NeoplasmsSentinel Lymph Node

Part of Cancer, Skin clinical trials.

This trial tests whether doing a sentinel lymph node biopsy later (after breast surgery) is a safe, accurate way to check if cancer has spread. It uses a special tracking shot that helps find the lymph nodes.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
500 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You have a pre-op diagnosis of ductal carcinoma in situ (DCIS), any grade and size
  • You are planning surgery that may include a risk-reducing mastectomy and a plan for sentinel lymph node biopsy (SLND) at your center
  • If your diagnosis was unclear or a higher-risk pre-cancer finding, your team is considering upfront SLND based on your test results
  • You are not pregnant and not breastfeeding
  • You do not have an allergy or intolerance to iron or the trial tracking medicine (including dextran or SPIO)
  • You do not have a condition that causes too much iron in the body

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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