πŸ›οΈ Verified NIH Record β€’ Updated 2025-12-23

Positron Lymphography Via Intracervical 18F-FDG Injection for Pre-surgical Lymphatic Mapping in Stage IB1 Cervical Cancer and High-grade Endometrial Cancer (NCT02285192)

πŸ”΅ Active, Not Recruiting Phase1 βš™οΈ Medical Device Protocol Sponsor: Memorial Sloan Kettering Cancer Center

🩺 Plain-English Summary (8th-Grade Level)

The purpose of this study is to see if a radioactive substance called 18F-Fluorodeoxyglucose (18F- FDG), injected into the cervix during a PET/CT scan done before surgery can show us more clearly which lymph nodes in the pelvis (the area near your uterus and cervix) contain cancer.

Who can join: Review the eligibility criteria below.

Location: Memorial Sloan Kettering Basking Ridge (Consent only) β€” Basking Ridge, New Jersey

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (7 Sites)

  • Memorial Sloan Kettering Basking Ridge (Consent only) β€” Basking Ridge, New Jersey
  • Memorial Sloan Kettering Monmouth (Consent only) β€” Middletown, New Jersey
  • Memorial Sloan Kettering Bergen (Consent only) β€” Montvale, New Jersey
  • Memorial Sloan Kettering Commack (Consent only) β€” Commack, New York
  • Memorial Sloan Kettering Westchester (Consent only) β€” Harrison, New York
  • Memorial Sloan Kettering Cancer Center β€” New York, New York
  • Memorial Sloan Kettering Nassau (Consent only) β€” Uniondale, New York

πŸ“ž Contact the Study Coordinator

Phone: (800) 525-2225

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Cervical Cancer clinical trials

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—