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Application of a novel,AI-based augmented reality navigation technique for intraoperative small pulmonary nodule localization: Prospective, Multi-center, Randomized, Controlled Trial

Application of a novel,AI-based augmented reality navigation technique for intraoperative small pulmonary nodule localization: Prospective, Multi-center, Randomized, Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112432
Enrollment
Unknown
Registered
2025-11-13
Start date
2025-03-05
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

small pulmonary nodule

Interventions

trial group:JediVision puncture navigation device assists in puncture
control group:Puncture under conventional CT guidance

Sponsors

Shanghai Geriatric Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old, gender not limited; 2. Confirmed by chest CT examination as a pulmonary nodule (diameter<= 2cm), and planned to undergo thoracoscopic resection; 3. Researchers determine that preoperative puncture positioning is necessary; 4. The subjects and their guardians are able to understand the research objectives, sign informed consent forms, and cooperate throughout the entire trial process.

Exclusion criteria

Exclusion criteria: 1. There are obvious enlarged lymph nodes in the hilum or mediastinum on chest CT examination; 2. Subjects who are not suitable for preoperative puncture positioning, such as pleural effusion, severe lung tissue damage, and pleural adhesions; 3. The subject has previously undergone chest surgery on the affected side; 4. Patients with important organ failure or other serious illnesses; 5. Pregnant and lactating women; 6. Participated in clinical trials of other drugs or medical devices during the same period 7. Other situations that the researcher deems unsuitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Positioning accuracy;

Secondary

MeasureTime frame
Auxiliary positioning operation time;Radiation exposure dose;

Countries

China

Contacts

Public ContactXuSongTao

Shanghai Geriatric Medical Center

xu.songtao@zs-hospital.sh.cn+86 135 0167 1739

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026