Actively Recruiting
Trans-Rectal Ultrasound of the Female Pelvis for Real-Time MRI-US Fusion Based Needle Tracking
Led by Duke University · Updated on 2026-03-06
17
Participants Needed
1
Research Sites
159 weeks
Total Duration
On this page
Sponsors
D
Duke University
Lead Sponsor
E
Eigen
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to utilize transrectal ultrasound (TRUS) images of the intact and post-hysterectomy female pelvis in order to provide feasibility information for a Magnetic Resonance Imaging (MRI)-TRUS fusion based 3D needle navigation system for use in image guided brachytherapy. The fusion and needle guidance will be performed using Eigen Health's navigation system that currently provides targeted MR/Ultrasound fusion based prostate biopsies utilizing a proprietary 3D semi-robotic navigation system.
CONDITIONS
Official Title
Trans-Rectal Ultrasound of the Female Pelvis for Real-Time MRI-US Fusion Based Needle Tracking
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Histologically proven invasive primary squamous, adenosquamous, or adenocarcinoma of the uterine cervix, or recurrent or medically inoperable uterine adenocarcinoma
- Treatment plan includes curative-intent definitive radiation with brachytherapy, with or without concurrent chemotherapy
- Adults 18 years of age or older
- ECOG Performance Status between 0 and 2
You will not qualify if you...
- Active rectal bleeding
- Presence of rectal ulcer
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Duke Cancer Center
Durham, North Carolina, United States, 27710
Actively Recruiting
Research Team
K
Kaitlin Bailey, BNS RN
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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