HYbrid RObotic Surgery MulTiCentric Study

NCT06849271 | Recruiting

• 1 other identifier: PL-PR01-150
• Study Type: interventional
• Target: 50
• Locations: 1 country
• Sites: 5

Brief Summary

The purpose of this clinical investigation, HYROS-MTC-I, is to confirm the effectiveness of the combined use of ROB-Bitrack System, its corresponding ElectroSurgical Endoscopic instruments and Non-ElectroSurgical Endoscopic instruments (ESE and NESE instruments respectively) and accessories in a multicentric study in urologic procedures with the indication of a robot assisted laparoscopic Radical/simple nephrectomy (RN), Partial nephrectomy (PN), Radical Prostatectomy (RP or P), and when it applies Lysis of Adhesions (during a PN, RN or RP or P to cut the adhesions and reach the organ) and Lymphadenectomy (only after a P with the aim to remove the lymph nodes) . HYROS-MTC-I is a confirmatory study in which the hypothesis of the primary endpoint is that: "Operative time (OT) with Bitrack System and its ESE/NESE Instruments and accessories will be equal or lower than superiority margin time of State of the Art (SoTA) of MIRS (Minimally Invasive Robotic Surgery) independently of the user experience and site". This study includes the data collected up to 30 days post-surgery.

Conditions

Nephrectomy; Prostatectomy

Keywords

Radical nephrectomy; Partial nephrectomy; Radical prostatectomy; Lymphadenectomy; Lysis of adhesions; Robotic surgery; Minimal Invasive surgery; Minimal Invasive robotic surgery; Urology

Outcome Measures

Primary Outcomes (1)

• Operative time (OT) with ROB-Bitrack System and its ESE/NESE Instruments and accessories to perform the surgeries.

  Evaluation of Operative time from first skin incision to last skin suture of the procedure.It is hypothesized that Operative time (OT) will be equal or lower than the maximum time as defined by the State of the Art (SoTA) of MIRS independently of the user experience and site.

  During the procedure

Study Arms (1)

Patients surgically treated with ROB-Bitrack System and ESE/ NESE instruments and accessories

EXPERIMENTAL

Procedure: Radical Nephrectomy (RN); Procedure: Partial nephrectomy (PN); Procedure: Radical Prostatectomy (RP)

Interventions

Radical Nephrectomy (RN) PROCEDURE

Complete remove of the kidney. In addition as part of the intervention, a procedure termed "Lysis of abdominal adhesions" may be performed according to patient medical condition and/or surgeon criteria.

Patients surgically treated with ROB-Bitrack System and ESE/ NESE instruments and accessories

Partial nephrectomy (PN) PROCEDURE

Partial remove of a section in the kidney. In addition, as part of the intervention, a procedure termed "Lysis of abdominal adhesions" may be performed according to patient medical condition and/or surgeon criteria.

Patients surgically treated with ROB-Bitrack System and ESE/ NESE instruments and accessories

Radical Prostatectomy (RP) PROCEDURE

Complete remove of the prostate gland. In addition as part of the intervention, two procedures termed "Lysis of abdominal adhesions" and/or "Lymphadenectomy " (removal of regional lymph nodes) may be performed according to patient medical condition and/or surgeon criteria.

Patients surgically treated with ROB-Bitrack System and ESE/ NESE instruments and accessories

Eligibility Criteria

• Age: 18 Years - 90 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Adult subjects between 18 and 90 years old who have provided written informed consent prior to any clinical investigation related procedures.
• Subjects who have been scheduled for a laparoscopic Radical/simple Nephrectomy surgery, laparoscopic Partial Nephrectomy or laparoscopic Radical Prostatectomy following the surgeon criteria.
• Ability and willingness to comply with all study requirements to be evaluated for each study visit.

You may not qualify if:

• Pregnant or breastfeeding women at the time of the surgery.
• Subjects with severe concomitant illness that, at PrincipaI investigator´s discretion, increases risk of therapeutic interventions or that have been submitted to multiple prior surgeries.
• Subjects admitted to the hospital due to an emergency situation.
• Subjects with untreated active infection.
• Subject with known allergy to some of the device components (i.e., stainless steel, etc.)
• Subjects not suitable to undergo Minimally Invasive Surgery (MIS)/ Minimally Invasive Robotic Surgery (MIRS), according to medical criteria.
• Subjects with life expectancy inferior to 3 months.
• Subjects with a BMI (Body Mass Index) ≥ 40
• Subjects with any contraindication for the use of the ROB-Bitrack System and the ESE/NESE instruments, as specified in the Instructions For Use.
• Subjects with abuses of active substances or with uncontrolled psychiatric disorders.
• Subjects with severe cardiopulmonary or coronary artery disease, bleeding disorders or that have been submitted to multiple prior operations.
• Subjects scheduled for surgeries intended to be in direct contact with the heart, the central circulatory system or the central nervous system.
• Inability to adhere to study-related procedures.
• Subjects who participate in another trial which may affect the outcome data on this study or the ability to complete the follow up requirements

Sponsors & Collaborators

• Rob Surgical Systems S.L.: lead

Study Sites (5)

Hospital del Mar

Barcelona, Spain, 08003, Spain

RECRUITING

Hospital Clinic de Barcelona

Barcelona, Spain, 08036, Spain

RECRUITING

Hospital General de Granollers

Granollers, Spain, 08402, Spain

RECRUITING

Hospital de Mataró

Mataró, Spain, 08304, Spain

RECRUITING

Hospital Universitari de Vic

Vic, Spain, 08500, Spain

RECRUITING

Central Study Contacts

Jaume Amat CEO

CONTACT

+34 930130883; jaume.amat@robsurgical.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Single Group Assignment

Study Record Dates

• First Submitted: January 9, 2025
• First Posted: February 27, 2025
• Study Start: January 15, 2025
• Primary Completion: November 1, 2025
• Study Completion: December 1, 2025
• Last Updated: July 31, 2025

Record last verified: 2025-07

Locations

ES (5)