- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04551235
Establishing Automatic Method of Counting and Classify Bone Marrow and Peripheral Blood Cells
March 9, 2022 updated by: National Taiwan University Hospital
Counting and classification of blood cells in a bone marrow smear and peripheral blood smear are essential to clinical hematology.
To this date, this procedure has been carried out in a manual manner in the great majority of clinical settings.
There is often inconsistency in the counting result between different operators largely due to its manual nature.
There has not been an effective and standard method for blood smear preparation and automatic counting and classification.
The recent advent of deep neural network for medical image processing introduced new opportunities for an effective solution of this long-standing problem.
Numerous results have been published on the effectiveness of convolutional neural network in clinical image recognition task.
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
900
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: Bor-Sheng Ko
- Phone Number: 886-0-72651297
- Email: kevinkomd@gmail.com
Study Locations
-
-
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Taipei, Taiwan
- Recruiting
- National Taiwan University Tai-Chen Cell Therapy Center
-
Contact:
- Bor-Sheng Ko
- Phone Number: 886-9-726512
- Email: kevinkomd@gmail.com
-
-
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.
Eligibility Criteria
Ages Eligible for Study
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients who have suspected or confirmed hematological diseases and receive bone marrow or peripheral blood cell morphological examination in National Taiwan University Cancer Center
Description
Inclusion Criteria:
- Patients who have suspected or confirmed hematological diseases and receive bone
- marrow or peripheral blood cell morphological examination in National Taiwan University Cancer Center
- Patients who are aged more than 20 y/o
Exclusion Criteria:
•Patients who are not willing to sign informed consents
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Evaluate the accuracy of cell counting and classifying between automatic method and manual method through digital microscopic photos of bone marrow smear and peripheral blood smear using deep convolutional neural networks
Time Frame: 3 years
|
3 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 Major Dates
Study Start (Actual)
August 28, 2020
Primary Completion (Anticipated)
December 31, 2023
Study Completion (Anticipated)
December 31, 2023
Study Registration Dates
First Submitted
August 27, 2020
First Submitted That Met QC Criteria
September 10, 2020
First Posted (Actual)
September 16, 2020
Study Record Updates
Last Update Posted (Actual)
March 10, 2022
Last Update Submitted That Met QC Criteria
March 9, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202007086RIPB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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