Identification of Fatty Liver With Advanced Fibrosis in Type 2 Diabetes Using Simple Fibrosis Scores and Electronic Reminder Messages
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- STATUS
- Recruiting
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- participants needed
- 952
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- sponsor
- Chinese University of Hong Kong
Summary
Description
This will be a parallel group, randomized controlled trial. Patients fulfilling the inclusion
and exclusion criteria above will be randomized 1:1 to two groups. Randomization will be
carried out through the use of computer-generated list of random numbers in variable blocks
of 4 to 10. Concealment of group allocation will be achieved through putting the group
allocation cards in consecutively-numbered and sealed envelopes. The patients and physicians
will know that the patients are in the intervention group if they see the reminder messages.
When they do not see a reminder message, there will not be a specific indicator of whether
the patient is in the control group or in the intervention group but having low
For patients in the intervention group, we will calculate the
"This patient has high Fibrosis-4 index (and/or AST-to-platelet ratio index) of xxx
suggestive of significant
The reminder message will pop up when physicians see the patient at the clinic and use the electronic clinical management system. The message will remain active for one year. Although the message is entered manually at this stage, the arrangement mimics an automated computer system. If the study results are positive, the next step is to modify the system to automate the process.
Patients in the control group will undergo the same assessments as patients in the
intervention group. Although physicians will have access to the raw liver biochemistry
results and
Details
Condition |
NIDDM, |
---|---|
Age | 18years - 70years |
Treatment |
Simple |
Clinical Study Identifier | NCT04241575 |
Sponsor | Chinese University of Hong Kong |
Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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