Trial · NCT07899931
Vision-Language-Based Large-Scale Model for Emergency Screening
NCT07899931, Not applicable, Recruiting, The First Hospital of Jilin University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Vision-Language-Based Large-Scale Model for Emergency Screening. Trials, record NCT07899931. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07899931
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Vision-Language-Based Large-Scale Model for Emergency Screening
- NCT number
- NCT07899931
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 640 participants, estimated
- Lead sponsor
- The First Hospital of Jilin University
- Conditions
- Acute Thoraco-Abdominal Emergency Lesions
- Interventions
- powER vision-language large-model assisted CT reading, Conventional CT reading without AI assistance
- First posted
- 2026-10-28
- Last updated
- 2026-10-28
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Per-case CT diagnostic decision time | Day 1 (at completion of CT image reading) | Time interval from opening the emergency thoraco-abdominal CT case on the reading platform to completion of critical lesion selection for diagnostic decision-making. This outcome compares the powER vision-language large-model assisted reading group with the conventional radiological reading group. |
| Secondary | Sensitivity for detecting critical emergency lesions on emergency thoraco-abdominal CT | up to 60 days | Sensitivity for detection of critical emergency lesions (including hemorrhage, visceral perforation, aortic dissection, etc.) on emergency thoraco-abdominal CT. The 60-day comprehensive clinical, surgical and pathological findings after randomization serve as the reference gold standard. This outcome compares powER vision-language large-model assisted radiological reading with conventional radiological reading. |
| Other | Specificity for detecting critical emergency lesions on emergency thoraco-abdominal CT | up to 60 days | Specificity for detection of critical emergency lesions on emergency thoraco-abdominal CT. The 60-day comprehensive clinical, surgical and pathological findings after randomization serve as the reference gold standard. This outcome compares powER vision-language large-model assisted radiological reading with conventional manual radiological reading. |
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/NCT07899931
GET https://conductscience.org/api/trials/v1/NCT07899931/registered