Clinical Trial Record

Return to Clinical Trials

The Application of DNA Nanomachines for Detecting microRNA in Blood for the Diagnosis of Pancreatic Cancer. Diagnosis of Pancreatic Cancer


2024-07-06


2025-06-01


2026-06-01


30

Study Overview

The Application of DNA Nanomachines for Detecting microRNA in Blood for the Diagnosis of Pancreatic Cancer. Diagnosis of Pancreatic Cancer

Previous research has shown that microRNAs in the blood can serve as biomarkers for early pancreatic cancer, with potential applications including detection, differential diagnosis, and prognosis prediction of pancreatic cancer. The current primary method for detecting microRNAs is RT-qPCR, but this process requires repeated temperature cycling, which demands high precision from the equipment. As an alternative, isothermal nucleic acid amplification technology does not require expensive temperature control instruments. Our research team has developed various isothermal nucleic acid amplification strategies for microRNA sensing platforms, applied to biological sample detection. This study combines the circular strand displacement amplification strategy with DNA nanomachines to develop a fluorescence sensing platform that performs dual signal amplification at a constant temperature. It is designed to detect pancreatic cancer-related microRNAs, exploring its role and potential applications in the diagnosis of pancreatic cancer patients.

N/A

  • Pancreas Adenocarcinoma
  • MicroRNA
  • GENETIC: MicroRNA (mir-642b-3p)
  • 202405082RINB

Study Record Dates

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

2024-07-05  

N/A  

2024-07-05  

2024-07-05  

N/A  

2024-07-12  

2024-07-12  

N/A  

2024-06  

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

Primary Purpose:
N/A


Allocation:
N/A


Interventional Model:
N/A


Masking:
N/A


Arms and Interventions

Participant Group/ArmIntervention/Treatment
: Pancreatic adenocarcinoma

Pancreatic adenocarcinoma which are proven by pathology, before initiation of anti-cancer treatment.

GENETIC: MicroRNA (mir-642b-3p)

  • A circulating microRNA in the blood of pancreatic cancer patients.
: Healthy control

People who do not have pancreatic disease.

Primary Outcome MeasuresMeasure DescriptionTime Frame
Ratio of the target microRNA in patients with and without pancreatic adenocarcinoma.24 hours
Secondary Outcome MeasuresMeasure DescriptionTime Frame

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Name: Weng Fai Wong, Master of Science

Phone Number: 886-972652272

Email: 106290@ntuh.gov.tw

Participation Criteria

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:
20 Years

Accepts Healthy Volunteers:
1

    Inclusion Criteria:

  • Pancreatic ductal adenocarcinoma
  • Proven by pathology
  • Patients who have not received anti-cancer therapies

  • Exclusion Criteria:

  • Less than 20 years old
  • Unable to provide inform and consent
  • Patients who have active malignancy other than pancreatic adenocarcinoma
  • Patients who have had pancreatic cancer whose anti-cancer therapies are completed or undergoing
  • Life expectancy less than 3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications

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