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Ceevra Reveal for Prostate Cancer
N/A
Waitlist Available
Led By James Porter, MD
Research Sponsored by Ceevra, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up measured 1-2 weeks after discharge
Awards & highlights
Study Summary
This study is evaluating whether a new type of surgery can be performed more efficiently.
Eligible Conditions
- Prostate Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ measured 1-2 weeks after discharge
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~measured 1-2 weeks after discharge
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Total operative time
Secondary outcome measures
Blood loss (measured in cubic centimeters)
Intraoperative complication
Intraoperative conversion from robotic assisted laparoscopic procedure to open procedure
+8 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Experimental: Intervention ArmExperimental Treatment1 Intervention
Subjects whose surgeon will be viewing VR models in addition to the source CT/MR image in connection with the case.
Group II: Control ArmActive Control1 Intervention
Subjects whose surgeon will only be viewing CT/MR images in connection with the case.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Ceevra Reveal
2017
N/A
~100
Find a Location
Who is running the clinical trial?
Ceevra, Inc.Lead Sponsor
2 Previous Clinical Trials
132 Total Patients Enrolled
1 Trials studying Prostate Cancer
40 Patients Enrolled for Prostate Cancer
James Porter, MDPrincipal InvestigatorSwedish Medical Center
2 Previous Clinical Trials
489 Total Patients Enrolled
1 Trials studying Prostate Cancer
300 Patients Enrolled for Prostate Cancer
Raymond Pak, MDPrincipal InvestigatorMayo Clinic
Frequently Asked Questions
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