Trial · NCT07885007
AI-SC Multi-center Study
NCT07885007, Active not recruiting, University Health Network, Toronto
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. AI-SC Multi-center Study. Trials, record NCT07885007. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07885007
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- AI-SC Multi-center Study
- NCT number
- NCT07885007
- Status
- Active not recruiting
- Enrollment
- 1,000 participants, estimated
- Lead sponsor
- University Health Network, Toronto
- Conditions
- Liver Cirrhosis
- Interventions
- evaluate the alignment between AI-SC recommendations and LT-SC decisions, Multi AI-SC model
- First posted
- 2026-10-21
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Concordance of AI-SC vs LT-SC review | 3 months | · Our primary outcome will be any substantial change in the content, method, or result of the patient assessment between the AI-SC and conventional reports. Investigators will calculate the percentage of concordance between the two, and the similarity of report generated by the human and the AI-SC will be evaluated using ROUGE score (Recall-Oriented Understudy for Gisting Evaluation), a quantitative metric that assesses textual similarity3. |
| Primary | Concordance between AI-SC vs LT-SC | 3 months | Our primary outcome will be any substantial change in the content, method, or result of the patient assessment between the AI-SC and conventional reports. Investigators will calculate the percentage of concordance between the two, and the similarity of report generated by the human and the AI-SC will be evaluated using ROUGE score (Recall-Oriented Understudy for Gisting Evaluation), a quantitative metric that assesses textual similarity3 |
| Secondary | Time of adjudication | 3 months | • The secondary outcomes will be the safety of assessments in cases where substantial changes are made, time required for adjudications, frequency of decision changes between AI-SC and conventional LT-SC. Investigators will also evaluate the consistency of the decision making across controversial variables, such as age, cardiovascular health, and frailty over time, to evaluate whether AI-SC can provide more objectivity in the decision-making. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07885007
GET https://conductscience.org/api/trials/v1/NCT07885007/registered