🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT06831617
Starting soon Not applicable

AI-based Low Dose CBCT Reconstruction for Clinical Application

NCT06831617 · tracked via the Priya Life Science China tracker
Sponsor
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Phase
Not applicable
Started
2025-03-01
Last updated
2025-02-18

Condition(s) studied

Lung Nodule

Investigational drug(s) / intervention(s)

AI-based low dose CBCT reconstructed images systemConventional CBCT images system

AI-based low dose CBCT reconstructed images system: Participants in the experimental group undergo AI-based low dose (radiation dose is 1/6th of the dose used in the clinic) CBCT reconstructed images guided lung puncture procedures.

Conventional CBCT images system: Participants in the experimental group undergo conventional CBCT images guided lung puncture procedures.

Study summary

The goal of this clinical trial is to learn if AI-based low dose CBCT reconstructed images can guide lung puncture effectively. The main questions it aims to answer are:

1. Does the AI-based low dose CBCT reconstruction model reconstruct high quality images?
2. Is it possible that low-dose CBCT reconstructed images can guide lung puncture procedures without compromising the efficiency of the procedure? Researchers will compare AI-based low dose CBCT reconstructed images to a placebo (conventional CBCT images) to see if AI-based low dose CBCT reconstructed image can guide lung puncture procedures without compromising the efficiency of the procedure.

Participants will:

1. Undergo lung puncture under AI-based low dose CBCT reconstructed images guidance or under conventional CBCT images
2. Be followed up for 1 week postoperative to obtain patient complications

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Participants who require CBCT-guided precutaneous lung puncture (PLP) and meet the clinical indications for the procedure. * Participants whose physical condition is suitable for PLP. * Participants are willing to sign informed consent. Exclusion Criteria: * Participants have metallic implants in the body, which severely affects the image quality. * Participants are pregnant or breastfeeding. * Participants are unwilling or unable to sign informed consent.

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
Wuhan Union Hospital Wuhan Hubei
Wuhan Union Jinyinhu Hospital Wuhan Hubei
Wuhan Union West Hospital Wuhan Hubei

More Union Hospital, Tongji Medical College, Huazhong University of Science and Technology trials in China

Other trials for the same condition

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 NCT06831617 on ClinicalTrials.gov ↗ ← All trials in China