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The Efficiency of Writing Endoscopic Reports by Artificial Intelligence and Physicians: a Randomized Controlled Trial

The Efficiency of Writing Endoscopic Reports by Artificial Intelligence and Physicians: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04275609
Enrollment
80
Registered
2020-02-19
Start date
2020-02-20
Completion date
2020-03-30
Last updated
2020-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastrointestinal Disease

Keywords

Endoscopic Report, Artificial Intelligence, Gastrointestinal Disease, Writing Efficiency

Brief summary

The purpose of this study is to compare the efficiency of writing endoscopic reports by artificial intelligence and physicians through a randomized controlled trial.

Detailed description

Digestive endoscopy permits early detection of gastrointestinal diseases and improving the patients' quality of life. However, writing endoscopic report takes a lot of manpower and time, reducing the efficiency of endoscopy. Our center has developed a structured diagnostic report generation system for digestive endoscopy, which can generates the report by artificial intelligence. Here, we compare the efficiency of writing endoscopic reports by artificial intelligence and physicians through a randomized controlled trial.

Interventions

OTHERAI generated report

After the endoscopic procedure, the physicians click the structured reporting button of computer to automatically complete the report through the structured diagnostic report generation system. The physicians only make minor corrections to the report.

OTHERphysicians writing report

After the endoscopic procedure, the physicians writing the report in computer according the procedure.

Sponsors

Shandong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* patients aged between 18 and 80 years; * patients undergoing gastroscopy and colonoscopy examination with anesthesia; * patients able to give informed consent

Exclusion criteria

* patients with the contraindications to endoscopic examination; * a history of gastrointestinal cancers; * allergic to anaesthetics in previous medical history; * the endoscopic procedure cannot be completed due to stenosis, obstruction, solid food or complications of anaesthesia.

Design outcomes

Primary

MeasureTime frameDescription
The time spent writing reportsIntraoperativeSum of the time for writing gastroscopic report and colonoscopic report。

Contacts

Primary ContactXiuli Zuo, MD,PhD
zuoxiuli@sdu.edu.cn15588818685

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026