Focused Ultrasound for the Treatment of Pancreatic Cancer - an International Registry

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20+
SponsorNational Taiwan University Hospital

About this trial

The purpose of the registry is to collect data on the performance of the focused ultrasound (FUS) technology and health outcomes. A wide variety of approaches exist for using FUS on pancreatic cancer patients, and the primary goal is to capture this broad spectrum of approaches and their impact on patients overall health. This information will help provide a better understanding of current care, and may possibly direct further, more specific investigations that will follow this registry.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

20 years and older

Provision of signed and dated informed consent form

Stated willingness to comply with all registry procedures and availability for the duration of the registry

Histology proven pancreatic carcinoma in any area of pancreas

Disqualifiers

Any disease, condition or surgery which would result in a contraindication to undergoing FUS therapy.

Clinical trials of pancreatic cancer not of focused ultrasound or related activities

Trial population

The registry will be implemented at approximately 10 sites internationally. In order to achieve the target registry population of 30 participants over 12 months in the NTUH site, participants who receive focused ultrasound for pancreatic cancer. Participant enrollment will be evaluated on a site by site basis throughout the enrollment period to provide diversity of participant and system representation.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Pain related to pancreatic cancer

Brief Pain Inventory from 0 (no pain) to 10 (pain as a bad as can imagine)

Time frame
after high focused ultrasound treatment, an average of 1 month
2

To observe the efficacy of local tumor ablation

the assessment of the tumor burden after high focused ultrasound treatment

Time frame
after high focused ultrasound treatment, an average of 1 month
3

The effect of local tumor ablation

time-to-progression

Time frame
over 12 months
4

To observe the survival rate

overall survival (OS)

Time frame
over 12 months

Secondary outcomes

Other outcomes

1

Impact on Quality of Life and Cost

Standardized instrument to measure of health-related quality of life.

Time frame
over 12 months

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: