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Diagnostic Accuracy of Robotically Assisted Cranial Biopsies Using Cirq Active Cranial and Automatic Image Registration

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

This is an observational post-market study determining biopsy accuracy in a clinical environment using Cirq® Robotic Alignment Module Cranial. The goal is to determine whether the robotic procedure to be examined can achieve a clinically acceptable value of at least 90% in terms of diagnostic yield.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Intracranial lesion and the indication for a diagnostic stereotactic biopsy validated by the neurosurgical staff

• Ability to consent to the procedure

Locations
Other Locations
France
The Centre Hospitalier Universitaire (CHU) d'Angers health establishment
RECRUITING
Angers
Contact Information
Primary
Christine M Bayer, PhD
christine.bayer@brainlab.com
+49 89 99 15 68
Time Frame
Start Date: 2023-11-01
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 50
Treatments
Biopsy Patient
Patient with a confirmed intracranial neoplasm scheduled for a biopsy with Cirq® Robotic Alignment Module Cranial and registration via Auto-Registration Software Universal Automatic Image Registration Cranial and Loop-X® Mobile Imaging Robot.
Related Therapeutic Areas
Sponsors
Leads: Brainlab AG

This content was sourced from clinicaltrials.gov