2019-02-01
2026-12
2026-12
30
NCT03820661
University Health Network, Toronto
University Health Network, Toronto
INTERVENTIONAL
High Resolution Ultrasound in Pancreatic Ductal Adenocarcinoma
Pancreatic cancer patients at UHN who have had a CT at UHN and have surgery planned will undergo a high resolution ultrasound pre-operatively and intra-operatively. This study is being done to see if using high resolution ultrasound before and during surgery will help the doctors accurately diagnose pancreatic ductal adenocarcinoma and identify if the disease has spread to other areas of the body.
N/A
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates | Results Reporting Dates | Study Record Updates |
---|---|---|
2019-01-11 | N/A | 2024-10-07 |
2019-01-25 | N/A | 2024-10-10 |
2019-01-29 | N/A | 2024-10 |
This section provides details of the study plan, including how the study is designed and what the study is measuring.
Primary Purpose:
Diagnostic
Allocation:
Na
Interventional Model:
Single Group
Masking:
None
Arms and Interventions
Participant Group/Arm | Intervention/Treatment |
---|---|
OTHER: High Resolution Ultasound Diagnostic high resolution ultrasound pre-operatively and intraoperatively | DEVICE: Ultrasound
|
Primary Outcome Measures | Measure Description | Time Frame |
---|---|---|
High-resolution U/S will be used to measure vascular invasion and regional lymph node metastases in PDAC | The U/S results will be compared to pre-operative CT scan to help determine the diagnostic effectiveness of High Resolution US | within 2 weeks of surgery |
Secondary Outcome Measures | Measure Description | Time Frame |
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This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.
Ages Eligible for Study:
ALL
Sexes Eligible for Study:
18 Years
Accepts Healthy Volunteers:
This is where you will find people and organizations involved with this study.
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
No publications available
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