ποΈ 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)
π΅ Active, Not Recruiting Phase1 βοΈ Medical Device Protocol Sponsor: Memorial Sloan Kettering Cancer Center
π©Ί 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
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π 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
π 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.
π° 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.
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π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.