Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
ID04705467

A Multi-Modality Comparison of Needle Placement During Gynecological Brachytherapy Procedures

Led by Western University, Canada · Updated on 2025-04-13

35

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the use of 3D ultrasound imaging during brachytherapy treatment for gynecological cancers, including primary or recurrent vaginal, endometrial, and cervical cancers. This study aims to improve needle placement accuracy in interstitial or intra-cavitary brachytherapy, which is important for delivering adequate radiation doses to tumors while protecting healthy pelvic organs. Currently, there is no standard real-time image guidance for needle insertion in these procedures, which this research seeks to address. The study involves patients receiving gynecological brachytherapy using a device-based approach, where needles and applicators are inserted under general anesthesia with guidance from clinical exams and pre-procedure MRI. An investigational 3D ultrasound device will be used during the procedure to provide real-time volumetric imaging of needle pathways, improving upon the limitations of standard 2D ultrasound. After the procedure, CT scans are performed for radiation planning. Participants will undergo imaging assessments including MRI before treatment and CT after treatment, with the main focus on measuring the accuracy of needle placement over a 16-month period. The study team will evaluate how effectively the 3D ultrasound helps avoid needle insertion into pelvic organs and optimizes tumor dose coverage. Patient safety and treatment monitoring will be conducted alongside these measurements within the study timeline.

CONDITIONS

Brief Title

3DUS Imaging of Needles in Gynecological Brachytherapy

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female aged 18 years or older
  • Patients with locally advanced or recurrent gynecological cancers
  • Offered interstitial or ring and tandem brachytherapy treatment
  • Includes vaginal, endometrial, or cervical cancers with adenocarcinoma or squamous cell carcinoma histologies
Not Eligible

You will not qualify if you...

  • Patients not offered interstitial brachytherapy as a treatment option

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Single procedure day

Participants undergo gynecological brachytherapy treatment involving needle and applicator insertion using investigational 3D ultrasound imaging to guide needle placement during the procedure.

1 procedure visit (in-person)

Post-operative Follow-up

Duration - Up to 16 months

Participants receive post-procedure CT imaging for radiation planning and assessment following brachytherapy treatment.

Follow-up visits as scheduled for up to 16 months

Trial Site Locations

Total: 1 location

1

London Regional Cancer Program, Victoria Hospital

London, Ontario, Canada, N6A 5W9

Actively Recruiting

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Research Team

D

David D'Souza, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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