Robotic assistance for endoscopic neurosurgery
Intraoperative Application of a Robot for Endoscopic Neurosurgical Interventions: A Prospective Study
This study is testing whether a robot can help doctors perform brain surgeries more accurately and safely by guiding them in real time during procedures like removing pituitary tumors.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 19 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Medical University of Graz Academic / other |
| Locations | 1 site (Graz, Styria) |
| Trial ID | NCT06311266 on ClinicalTrials.gov |
What this trial studies
This study evaluates the use of the EndoGuide robot, a modular positioning device designed to enhance the precision of endoscopic neurosurgical interventions. By utilizing radiological data from neuronavigation, the robot aims to align the surgical trajectory in real time with an accuracy of less than 0.1mm. The focus is on procedures such as transnasal pituitary adenoma resection and ventriculostomy, which are common neurosurgical interventions. The goal is to improve surgical outcomes by reducing complications associated with manual guidance during these delicate procedures.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18-80 with specific diagnoses requiring ventriculostomy or transsphenoidal surgery.
Not a fit: Patients who are pregnant, breastfeeding, or unable to provide informed consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance the accuracy of neurosurgical interventions and reduce patient morbidity.
How similar studies have performed: Previous studies have shown promising results with robotic assistance in surgical procedures, indicating potential for success in this novel application.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Written informed consent to participate in the present study * Procedure-related patient insurance * Age 18-80 years * Diagnosis indicating a ventriculostomy * Diagnosis of an endo- or suprasellar lesion with indication for transsphenoidal surgery * MRI and CT scanner compatible Exclusion Criteria: * Pregnancy, breast feeding * Patients not able to reason * Age \<18 or \>80 years * Claustrophobia
Where this trial is running
Graz, Styria
- Medical University of Graz — Graz, Styria, Austria (Recruiting)
Study contacts
- Study coordinator: Alexander SG Micko, MD, PhD
- Email: alexander.micko@medunigraz.at
- Phone: +4331638581257
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.