Anastomosis, Surgical

5

Review clinical trials related to Anastomosis, Surgical. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Post-market, Real-world Experience: Expanding Access to Care by Incorporating the Symani® Surgical System and Enabling Surgeons

The objective of this study is to evaluate the Symani System's safety and effectiveness for microsurgical anastomosis during free tissue transfer surgery and lymphovenous anastomosis surgery. The primary endpoints are: * Effectiveness- Rate of intraoperative anastomosis patency at first attempt. * Safety- Freedom from device-related adverse events. Participants will receive treatment as standard of care and be asked to: * Allow the researchers to access and use their information. * If participants are undergoing a lymphedema procedure, they will be asked to undergo a questionnaire as part of the study. * Participants will be asked to comply with the follow-up visits and complete all study procedures/questionnaires as outlined in the protocol.

Participants needed: 455
Trial details
Age: 22+Biological sex: AllType: ObservationalSponsor: MMI (Medical Microinstruments, Inc.)Updated: Jul 13, 2026Locations: 6
Eligibility criteria

At least 22 years of age [+9]

Patients who are incapable and/or unwilling to provide informed consent [+25]

Status: Recruiting

A Post-market, Real-world Experience: Expanding Access to Care by Incorporating the Symani® Surgical System and Enabling Surgeons

The objective of this study is to evaluate the Symani System's safety and effectiveness for microsurgical anastomosis during free tissue transfer surgery and lymphovenous anastomosis surgery. The primary endpoints are: * Effectiveness- Rate of intraoperative anastomosis patency at first attempt. * Safety- Freedom from device-related adverse events. Participants will receive treatment as standard of care and be asked to: * Allow the researchers to access and use their information. * If participants are undergoing a lymphedema procedure, they will be asked to undergo a questionnaire as part of the study. * Participants will be asked to comply with the follow-up visits and complete all study procedures/questionnaires as outlined in the protocol.

Participants needed: 455
Trial details
Age: 22+Biological sex: AllType: ObservationalSponsor: MMI (Medical Microinstruments, Inc.)Updated: Mar 5, 2026Locations: 4
Eligibility criteria

At least 22 years of age [+9]

Patients who are incapable and/or unwilling to provide informed consent [+25]

Status: Recruiting

MagDI U.S. Registry

Assess the incidence and severity of internal hernia and bowel obstruction at one year in a U.S. population following use of the MagDI System to create side-to-side duodeno-ileal anastomoses.

Participants needed: 106
Trial details
Age: 22+Biological sex: AllType: ObservationalSponsor: GT Metabolic Solutions, Inc.Updated: Feb 20, 2026Locations: 5Duration: 12 Months
Eligibility criteria

>21 years of age, at the time of informed consent. [+3]

Status: Not yet recruiting

Evaluation of MUSA-3 in Microsurgical Anastomoses

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

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: MicrosureUpdated: Feb 23, 2026
Eligibility criteria

Patient age ≥ 18 years. [+4]

Subject participates in a potentially confounding drug or device trial during th... [+4]

Status: Not yet recruiting

AUGUR-AI - Indocyanine Green Fluorescence Angiography Representer

Surgery can effectively treat colorectal cancer, but it is a complex procedure with risks and complications. Surgeons often rely on cameras to visually guide their instruments during operations, especially in minimally invasive ("keyhole") and endoscopic procedures. The camera is connected to a computer and generates the internal scene onto a display screen, which the surgeon looks at throughout the procedure, helping them make informed decisions throughout the operation. Fluorescence-guided surgery uses a particular type of camera that can detect images in both normal light and in the near-infrared range. To work, it needs the administration of an agent called indocyanine green to a patient and then the camera can see if the agent is in the tissue of interest to the operation at the time of the surgery. In this way, decisions regarding blood supply ("perfusion") can be helped, especially related to safety in joining together portions of tissue after removal of disease. The equipment and agent are approved for use in this way and have very good safety profiles. Many international studies have already demonstrated that the use of fluorescence-guided surgery is associated with lower rates of leaks when disease bowel segments are removed, and the healthy ends are joined back together. Previous work we have done has shown that sophisticated computing methods can learn to interpret the fluorescence patterns to a similar standard as a surgeon who is very experienced in fluorescence-guided surgery. In this study, we aim to assess whether the computer system we have developed work in real-time, in theatre to provide a reliable interpretation of the fluorescence pattern, that would match how an expert would interpret the same pattern. The system's analysis will not impact on the operation; instead, video images will be recorded, processed and analysed by our computer system. The results of the interpretation will not be shown to the operating surgeon during the procedure to avoid any impact on decision-making.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Mater Misericordiae University HospitalUpdated: Nov 27, 2024Locations: 1Duration: 90 Days
Eligibility criteria

Participant is willing and able to give informed consent for participation in th... [+5]

Participant who is pregnant, lactating or planning pregnancy during the course o... [+4]