Observing the use of the Maestro Platform in laparoscopic surgery
Maestro 1.1 Post-Market Registry
Moon Surgical · NCT06103136
This study looks at how well the Maestro surgical device works during laparoscopic surgeries to see if it can help improve patient outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 600 (estimated) |
| Ages | 18 Years to 100 Years |
| Sex | All |
| Sponsor | Moon Surgical (industry) |
| Locations | 12 sites (Denver, Colorado and 11 other locations) |
| Trial ID | NCT06103136 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather data on the real-life application of the Maestro Platform, a surgical assistance device, during laparoscopic surgeries. It will involve adult participants who are scheduled for such procedures, allowing researchers to assess the effectiveness and usability of the platform in a clinical setting. The study will not involve any experimental interventions but will focus on collecting observational data from various medical centers. The findings could provide insights into the platform's performance and potential improvements in surgical outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 years and older who are scheduled for laparoscopic surgery.
Not a fit: Patients who are not undergoing laparoscopic surgery or those excluded at the investigator's discretion may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the understanding of the Maestro Platform's effectiveness in improving surgical outcomes for patients undergoing laparoscopic procedures.
How similar studies have performed: While this study is observational and focuses on real-world usage, similar studies involving surgical assistance devices have shown promising results in improving surgical efficiency and outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants will be adults aged ≥ 18 years scheduled for laparoscopic surgery. Exclusion Criteria: * Participants might be excluded based on the investigator's discretion.
Where this trial is running
Denver, Colorado and 11 other locations
- Rose Medical Center — Denver, Colorado, United States (RECRUITING)
- Lee Health — Fort Myers, Florida, United States (RECRUITING)
- Baptist Health — Jacksonville, Florida, United States (RECRUITING)
- Baptist Medical Center Beaches — Jacksonville, Florida, United States (RECRUITING)
- Orlando Veterans Affairs Medical Center — Orlando, Florida, United States (RECRUITING)
- Surgeon's Point ASC — Cedar Park, Texas, United States (RECRUITING)
- Chirec Delta — Auderghem, Belgium (RECRUITING)
- Hôpital Privé Arnault Tzanck — Mougin, Alpes Maritimes, France (RECRUITING)
- Polyclinique de Franche-Comté — Besançon, France (RECRUITING)
- Clinique Bouchard — Marseille, France (RECRUITING)
- Institut Arnault Tzanck — Saint-Laurent-du-Var, France (RECRUITING)
- Clinique de l'Orangerie — Strasbourg, France (RECRUITING)
Study contacts
- Study coordinator: Anne Osdoit
- Email: aosdoit@moonsurgical.com
- Phone: 6 60 42 28 31
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Surgery, abdominal laparoscopic surgery, surgical assistance device