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Study of New Software Used During Ablations

Prospective Pilot Observational Study Examining Cone Beam CT and CT Thermometry During Ablations

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01906021
Enrollment
13
Registered
2013-07-23
Start date
2013-09-23
Completion date
2020-12-08
Last updated
2020-12-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatic Cancer, Hepatic Neoplasms, Liver Cancer, Neoplasms, Liver

Keywords

Thermomap, Hepatic Lesions, Radiofrequency Ablation, Microwave, Non-Invasive Technique

Brief summary

Background: \- Ablation is a procedure that heats tumor tissue to a high temperature to destroy it. Doctors perform this procedure by putting a probe in the tumor. This delivers heat to the site. Currently, doctors tell what area is heated by using the probe s manufacturer estimates. These estimates are imprecise. Doctors insert small needles to measure the temperature around the area being heated. Doctors also perform scans of the area, but these cannot show which tissue has been heated and which has not. Right now, only contrast scans can show that. But researchers have developed software that uses images from routine scans to create a temperature map. They want to test the software to see if doctors can monitor the procedure without using more needles and without contrast scans. Objectives: \- To test software that might help doctors perform ablations better in the future. Eligibility: \- People over 18 years of age already scheduled to have an ablation. Design: * Participants will be screened with a medical history. * Participants will visit the clinic for their already-scheduled ablation. The doctor will use the study software to analyze the temperature in the area being heated. The software will not come into contact with a participant s body. \- Participants will undergo scans that are necessary for the procedure, but one or two additional scans may be done as part of this study.

Detailed description

Background: * Lack of reliable non-invasive method to monitor ablation zone during radiofrequency or microwave ablation * Development of a non-invasive technique to examine temperature changes based on changes in CT or CBCT attenuation Objectives: -To measure accuracy of temperature monitoring using non-invasive thermomap (temperature imaging profile) method compared to the currently accepted invasive thermocouples method. Eligibility: * Subjects are eligible if: --They are scheduled in interventional radiology for hepatic radiofrequency or microwave ablation requiring thermocouples for monitoring * Subjects are excluded if they have: * An altered mental status precluding understanding or consenting for the procedure * A gross body weight exceeding 375 pounds (upper limit of angio table) * A pregnancy Design: * Number of participants: 16 * Number of sites: 1 * Recruitment time frame: 2 years * Type of study: pilot study to validate an image analysis thermometry technique * Patients undergoing clinically indicated hepatic ablations are eligible for this protocol. As part of this study, one to two additional research scans of the liver may be acquired during the ablation and analyzed separately with our software and compared with thermocouple measurements. There will be no changes in devices, probes or additional probe manipulations as part of this study. The operator will not modify the procedure based on results of this software.

Interventions

PROCEDURECT/CBCT thermometry method

The study consists of acquiring one or maximum two additional CT or CBCT of the liver during hepatic RFA or MWA and analyzing the images to obtain a temperature map

PROCEDUREAblation Probe

Temperature measured with thermocouples (current clinically approved method consisting of invasive needle placement for point measurement in area of concern)

Sponsors

National Institutes of Health Clinical Center (CC)
Lead SponsorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* INCLUSION CRITERIA: * Subjects must be scheduled for a hepatic radiofrequency or microwave ablation in interventional radiology requiring thermocouples for temperature monitoring. Any patient undergoing a hepatic radiofrequency or microwave ablation could be eligible for this protocol. * Must be age 18 years or older.

Exclusion criteria

* Subjects have an altered mental status precluding understanding or consenting to the procedure * Subjects have a body weight in excess of 375 lbs. * Subject is pregnant

Design outcomes

Primary

MeasureTime frameDescription
To measure accuracy of temperature monitoring using non-invasive thermomap (temperature imaging profile) method compared to the currently accepted invasive thermocouples methodtwo yearsBayesian median estimate will be used.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026