Pain Control for Breast Cancer Patients Receiving Injection of Radioactive Tracer
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Breast Cancer
- Breast Cancer - Female
- Breast Neoplasms
- Sentinel Lymph Node
- Type
- Interventional
- Phase
- Phase 3
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: There will be four separate treatment arms. Participants have equal chances of being assigned to any of the four arms.Masking: Single (Outcomes Assessor)Masking Description: Data will be analyzed with intervention arms masked.Primary Purpose: Supportive Care
Participation Requirements
- Age
- Between 18 years and 125 years
- Gender
- Only males
Description
Primary Objective: To test the effectiveness of four alternative approaches to topical anesthesia on pain associated with radiotracer injection for women diagnosed with breast cancer undergoing sentinel lymph node mapping. Secondary Objectives: To assess patient satisfaction with pain control modali...
Primary Objective: To test the effectiveness of four alternative approaches to topical anesthesia on pain associated with radiotracer injection for women diagnosed with breast cancer undergoing sentinel lymph node mapping. Secondary Objectives: To assess patient satisfaction with pain control modality for radiotracer injection. To identify barriers to implementation of the different pain control interventions.
Tracking Information
- NCT #
- NCT04822597
- Collaborators
- National Cancer Institute (NCI)
- Investigators
- Principal Investigator: Heather B Neuman, MD University of Wisconsin Madison School of Medicine and Public Health
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