Using ultrasonic scissors for lymph node removal in breast cancer patients
Economic Comparison Between the Use of Ultrasonic Scissors and Diathermy for Axillary Clearance in Breast Cancer Patients
This study tests whether using ultrasonic scissors for lymph node removal in breast cancer patients can lead to fewer complications and better recovery than traditional methods.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 150 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Linkoeping Academic / other |
| Locations | 1 site (Linköping, Östergötland) |
| Trial ID | NCT05901064 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of Harmonic Focus ultrasonic scissors compared to conventional diathermy for axillary clearance in breast cancer patients. The focus is on reducing complications such as seroma, infections, and the need for repeated drainage visits. The study is conducted at Linköping University Hospital, which performs around 60 axillary clearances annually. By evaluating the outcomes of these two surgical methods, the study aims to determine if ultrasonic scissors can improve patient recovery and reduce complications.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are scheduled for axillary evacuation due to breast cancer.
Not a fit: Patients who have previously undergone axillary evacuation will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to fewer complications and better recovery for breast cancer patients undergoing axillary clearance.
How similar studies have performed: While the use of ultrasonic devices in surgery is gaining traction, this specific comparison with diathermy is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years or older * All patients who will undergo axillary evacuation * Informed consent Exclusion Criteria: * Patients who have previously undergone axillary evacuation.
Where this trial is running
Linköping, Östergötland
- University hospital of Linkoping — Linköping, Östergötland, Sweden (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.