Not Yet RecruitingNot Applicable

Evaluation of MUSA-3 in Microsurgical Anastomoses

30 participantsStarted 2026-04-20

Plain-language summary

This study is conducted to evaluate the safety and performance of robot-assisted microsurgical anastomoses with the MUSA-3 system.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patient age ≥ 18 years. * Patients requiring procedures involving micro-anastomosis of small anatomical structures-such as blood vessels, nerves, or lymphatic vessels-in free flap, lymphatic, or peripheral nerve surgery. * Patients who have been selected by the research team at the Clinical Center as appropriate candidates for treatment with MUSA-3 in accordance with the IFU. * Able to give informed consent before participating in the study. * Provision of signed and dated informed consent form. Exclusion Criteria: * Subject participates in a potentially confounding drug or device trial during the course of the study. * Patients that are pregnant or breastfeeding. For Lymphedema patients: * ≥ISL (International Society of Lymphology) Stage III lymphedema * History of marcaine or indocyanine green allergy * Non-viable lymphatic system as determined by ICG lymphatic mapping using near infrared camera

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Safety: device-related adverse events (AEs)

Timeframe: Intraoperatively and through the 30-day post-procedure period

Performance: conversion rate to manual procedure

Timeframe: Intraoperatively

Clinical performance: vessel patency rate

Timeframe: Intraoperatively

Trial details

NCT IDNCT07427823

SponsorMicrosure

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2026-09-28

View on ClinicalTrials.gov More Anastomosis, Surgical trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.