CompletedNCT05255393
Survey on Lymphedema After Sentinel Lymph Node Biopsy in People With Cervical or Vulvar Cancer
Studying Vulvar carcinoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Memorial Sloan Kettering Cancer Center
- Principal Investigator
- Mario Leitao, MDMemorial Sloan Kettering Cancer Center
- Intervention
- Questionnaires(other)
- Enrollment
- 111 target
- Eligibility
- 18 years · FEMALE
- Timeline
- 2022 – 2025
Study locations (1)
- Memorial Sloan Kettering Cancer Center, New York, New York, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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