Robot vs scope: which minimally invasive surgery spares more nerves in breast cancer?
NCT ID NCT07693361
First seen Jul 09, 2026 · Last updated Jul 10, 2026 · Updated 1 time
Summary
This study compares two minimally invasive techniques for removing lymph nodes under the arm in people with breast cancer that has spread to those nodes. The goal is to see which method better protects nearby nerves, reduces side effects like numbness or pain, and improves recovery and quality of life. Researchers will review medical records from multiple hospitals to analyze outcomes such as nerve function, complications, and long-term cancer control.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If robotic surgery proves better at protecting nerves and reducing side effects, it could become the preferred minimally invasive option for lymph node removal in breast cancer.
- What could go wrong
- This is a retrospective study, meaning it looks back at medical records rather than testing treatments head-to-head in a controlled trial. Results may be influenced by unmeasured differences between patient groups.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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127 people
The number who actually took part.
- Started
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Oct 2021
- Expected to finish
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May 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with breast cancer who underwent either robotic-assisted or endoscopic-assisted axillary lymph node dissection at the Department of Breast and Thyroid Surgery Center, Guangzhou Medical University Affiliated Women and Children's Medical Center and Foshan Fosun Chancheng Hospital.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * pathologically confirmed breast cancer; * clinical N1-N3 stage or confirmation of lymph node metastasis by intraoperative frozen pathology; * Enlarged lymph nodes without significant adhesion to the axillary vessels or nerves; * Ability to comprehend the research questions; * Provision of informed consent and cooperation with the investigation; * No history or current diagnosis of mental illness or impaired consciousness; * ECOG PS 0-1. Exclusion Criteria: * Patients without lymph node metastasis; * Patients who refuse surgery; * Breast cancer patients with cognitive impairment, altered mental status, or inability to clearly express their feelings; * Critically ill patients; * Patients with other malignant tumors or severe medical conditions that render them unable to tolerate surgery.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Foshan Fosun Chancheng Hospital
Foshan, Guangdong, China
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Guangzhou Women and Children's Medical Center, Guangzhou Medical University
Guangzhou, Guangdong, 510000, China
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