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Clinical Trials in China / NCT07752862
Starting soon Observational

Prospective Collection and Registry Study of Multicenter, Multidisciplinary Surgical Minimally Invasive Videos

NCT07752862 · tracked via the Priya Life Science China tracker
Sponsor
Chinese Academy of Sciences
Phase
Observational
Started
2026-08-01
Last updated
2026-08-07

Condition(s) studied

Surgical NeoplasmsAbdominal Surgical DiseasesPelvic Surgical DiseasesUrologic Surgical DiseasesMusculoskeletal Surgical DiseasesHead and Neck Surgical DiseasesThoracic Surgical Diseases

Study summary

This is a prospective multicenter patient registry study. We continuously collect full-length intraoperative surgical videos from thoracoscope, laparoscope, hysteroscope, transcervical resectoscope, cystoscope, prostate resectoscope, arthroscope, intervertebral foramen endoscope, otorhinolaryngology endoscope and endoscopic surgical robots, accompanied by inpatient medical records, preoperative imaging data and 5-year postoperative follow-up data. All imaging data will be standardized and de-identified to construct a large-scale standardized surgical video dataset. The dataset will be applied for training, verification and optimization of surgical video foundation large model, serving for surgical teaching, intraoperative operation quality control and basic medical AI research. We will also explore the correlation between intraoperative surgical details and postoperative prognosis to improve the standard specifications of minimally invasive surgery. No clinical intervention will be imposed on participants throughout the whole research.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: 1. Patients aged ≥ 18 years old hospitalized to receive minimally invasive endoscopic, laparoscopic or robotic surgical treatment for diseases of various body systems; 2. Complete full-length intraoperative surgical videos can be recorded during operation, with complete medical records and preoperative imaging data; 3. Participants fully understand the study, voluntarily sign written informed consent, and agree that their de-identified intraoperative images and clinical data can be used for scientific research. Exclusion Criteria: 1. Minors under 18 years of age; 2. Patients with incomplete intraoperative videos or missing clinical imaging documents; 3. Patients with consciousness disturbance or mental disorders who cannot sign informed consent independently; 4. Subjects who refuse to participate in the study and disapprove the use of their medical data for research; 5. Patients who are predicted to be unavailable for long-term postoperative follow-up.

Primary outcome measure(s)

  • Completion rate of qualified intraoperative surgical imaging data — Immediately after each surgery

Trial sites (1)

FacilityCityRegionStatus
Institute of Automation, Chinese Academy of Sciences Beijing China

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07752862 on ClinicalTrials.gov ↗ ← All trials in China