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Trial Title:
Electrosurgical Bipolar Systems Versus Conventional Electrocautery After SLNBx
NCT ID:
NCT06426810
Condition:
Breast Cancer
Conditions: Official terms:
Breast Neoplasms
Study type:
Interventional
Study phase:
N/A
Overall status:
Recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Treatment
Masking:
Double (Participant, Outcomes Assessor)
Intervention:
Intervention type:
Device
Intervention name:
Electrosurgical bipolar system (LigaSure)
Description:
Study participants using a electrosurgical bipolar energy system will undergo sentinel
lymph node biopsy using only LigaSure during the surgery.
Arm group label:
Electrosurgical bipolar systems group
Summary:
The efficacy of electrosurgical bipolar systems in axillary lymph node dissection for
breast cancer surgery is well known. In this study, the investigators aim to determine
whether using electrosurgical bipolar systems helps reduce seroma formation in high-risk
patients undergoing sentinel lymph node biopsy (SLNB) for breast cancer surgery. The
investigators will focus on patients who are expected to experience high drainage output
after SLNB, especially those who are obese (BMI>25) or have undergone preoperative
chemotherapy.
Detailed description:
The most common complications of breast cancer surgery are lymphorrhea and seroma. Seroma
increases the length of hospital stay, the duration of outpatient treatment, and patient
discomfort. Persistent seroma can lead to re-hospitalization due to wound infection
caused by repeated aspirations. Seroma generally occurs in 10% to 85% of cases after
breast cancer surgery. Risk factors associated with seroma or lymphorrhea identified in
previous studies include age over 60, high BMI, tumor size, preoperative chemotherapy,
extent of breast tissue resection, number of lymph nodes removed, and number of lymph
node metastases.
Efforts to reduce seroma after breast cancer surgery include meticulous techniques such
as sharp dissection, the use of monopolar energy devices, and ligation of blood vessels
and lymphatics. Recently, the bipolar energy sealing system has been increasingly used.
LigaSure, which uses electric energy and pressure to denature collagen and elastin in
tissue, has been shown to reduce surgical time and medical costs compared to traditional
clamp-and-tie methods and advanced sealing systems in various surgeries, including breast
cancer.
In breast cancer surgery, using a electrosurgical bipolar systems for ligating blood
vessels and lymph nodes has several potential advantages. Traditional ligation using
sutures or monopolar energy devices can be influenced by surgical technique and has
drawbacks such as thermal injury to surrounding tissue. In contrast, the bipolar energy
sealer applies both electric energy and pressure simultaneously, minimizing thermal
injury to surrounding tissue while ensuring permanent vessel and lymphatic ligation.
A 2008 prospective study showed that using bipolar energy sealers in axillary dissection
allowed for earlier removal of drains compared to conventional methods. Other studies
have shown less blood loss, lower drainage output, and shorter hospital stays during
surgery. Recent research has also reported new applications of bipolar energy sealers in
skin-sparing mastectomy, indicating active use in breast surgery overseas. A study
conducted at Severance Hospital in South Korea found that using bipolar energy sealers
reduced drainage.
However, most of these studies were conducted abroad with a small number of reported
cases, and the results mainly concern axillary lymph node dissection (ALND), which is
where seroma is most often formed. With the decreasing trend of ALND due to advances in
preoperative chemotherapy and radiotherapy, there is a lack of studies on whether using
electrosurgical bipolar systems helps reduce seroma formation after sentinel lymph node
biopsy.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- Women aged 20-80
- Candidates for breast-conserving surgery and axillary sentinel lymph node biopsy
- BMI over 25 or those who have received preoperative chemotherapy
- Overall performance status of Eastern Cooperative Oncology Group (ECOG) 0-2
- Participants who understand the study contents and can provide written consent
- Participants without evidence of distant metastasis
Exclusion Criteria:
- Those with suspected axillary lymph node enlargement or metastasis on preoperative
imaging (breast MRI, chest CT, breast ultrasound)
- Among patients who had confirmed lymph node metastasis before neoadjuvant
chemotherapy, whose preopreative image showed residual disease at axillary lymph
node
- Those planning for mastectomy
- Those planning for axillary lymph node dissection without SLNBx
- Male breast cancer patients
- Patients with bilateral breast cancer
- Illiterate individuals, foreigners, or others who cannot read or understand the
consent form
- Individuals who voluntarily decide not to participate in the study or do not sign
the consent form
- Those judged by the researcher to be inappropriate for participation in this study
- Study participants who did not have a drain inserted in the surgical area
- If the randomized device is not used due to surgical room conditions (e.g.,
unavailability due to other emergency surgeries, device malfunction) and another
device is substituted
Gender:
Female
Minimum age:
20 Years
Maximum age:
80 Years
Healthy volunteers:
No
Locations:
Facility:
Name:
SMG-SNU Boramae medical center
Address:
City:
Seoul
Zip:
07061
Country:
Korea, Republic of
Status:
Recruiting
Contact:
Last name:
Jong-Ho Cheun, M.S.
Phone:
+82-10-8754-3054
Email:
chun89aaa@naver.com
Start date:
May 7, 2024
Completion date:
April 7, 2027
Lead sponsor:
Agency:
SMG-SNU Boramae Medical Center
Agency class:
Other
Source:
SMG-SNU Boramae Medical Center
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06426810