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NCT05255393 · ClinicalTrials.gov registry record
Survey on Lymphedema After Sentinel Lymph Node Biopsy in People With Cervical or Vulvar Cancer
A clinical trial of Cervical Cancer and Vulvar Cancer, sponsored by Memorial Sloan Kettering Cancer Center.
- Completed
- Registry status
- 111
- Enrollment target
- 1
- Study location
NCT05255393 is a study of Cervical Cancer and Vulvar Cancer that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 111 participants, below the 570-participant average among 144 other Cervical Cancer trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05255393, a study of Cervical Cancer and Vulvar Cancer, has completed, sponsored by Memorial Sloan Kettering Cancer Center.
- COMPLETED
- Registry status
- 111 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to collect information that may identify people who are at risk of developing lower extremity lymphedema (LEL) after sentinel lymph node biopsy (SLN) during surgery for early-stage vulvar or cervical cancer, and to improve the quality and accuracy of the information that is given to people who have this procedure. Please note that, during this study, the researchers will collect information from a questionnaire completed by people who had SLN and LND+/- SLN during surgery for early-stage cervical or vulvar cancer. No form of treatment will be provided as part of the study, and no investigational tests or procedures will be performed.
Conditions Studied
Interventions
- OTHER Questionnaires
Study Locations (1)
New York
- Memorial Sloan Kettering Cancer Center - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 111 participants |
| Start Date | 2022-02-15 |
| Est. Completion | 2025-11-19 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05255393
The ClinicalTrials.gov registry entry for NCT05255393 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 111 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 570-participant average among 144 other Cervical Cancer trials with a reported enrollment target (81% lower). The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Cervical Cancer appearing as the primary indexed condition, and to 1 intervention - of which Questionnaires is the first listed.
NCT05255393 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT05255393 about?
NCT05255393 is a clinical study titled "Survey on Lymphedema After Sentinel Lymph Node Biopsy in People With Cervical or Vulvar Cancer". The purpose of this study is to collect information that may identify people who are at risk of developing lower extremity lymphedema (LEL) after sentinel lymph node biopsy (SLN) during surgery for early-stage vulvar or cervical cancer, and to improve the quality and accuracy of the information that...
What is the current status of trial NCT05255393?
This trial is currently completed. The enrollment target is 111 participants. The study started on 2022-02-15. Estimated completion is 2025-11-19.
What conditions does trial NCT05255393 study?
This clinical trial studies the following conditions: Cervical Cancer, Vulvar Cancer.
What interventions are being tested in trial NCT05255393?
The interventions under investigation include: Questionnaires (OTHER).
Who is sponsoring clinical trial NCT05255393?
This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05255393 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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