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Clinical Trials/NCT06507774
NCT06507774
Active, not recruiting
Not Applicable

Development Project of AI and CAD-Assisted Multi-Material 3D Printing and Multi-Modal 3D Modeling Precision Multi-Organ Surgical Planning Model

Yangdi1 site in 1 country300 target enrollmentJanuary 1, 2023
ConditionsLung Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lung Cancer
Sponsor
Yangdi
Enrollment
300
Locations
1
Primary Endpoint
Blood Loss
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

This project focuses on the development of a precision multi-organ surgical planning model aided by artificial intelligence (AI), computer-aided design (CAD), multi-material 3D printing, and multimodal 3D modeling. The integration of these advanced technologies aims to enhance the accuracy and efficiency of preoperative planning for complex surgical procedures involving multiple organs. By leveraging AI and CAD, the project seeks to create detailed, patient-specific 3D models that incorporate various imaging modalities. These models will be used to guide multi-material 3D printing, producing highly accurate replicas of anatomical structures. The ultimate goal is to improve surgical outcomes by providing surgeons with precise and comprehensive tools for planning and executing intricate surgeries.

Registry
clinicaltrials.gov
Start Date
January 1, 2023
End Date
December 31, 2025
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Yangdi
Responsible Party
Sponsor Investigator
Principal Investigator

Yangdi

Sponsor-Investigator / Student

Affiliated Hospital of Hebei University

Eligibility Criteria

Inclusion Criteria

  • Patients diagnosed with lung cancer Complete clinical case data; All patients underwent surgical treatment; Voluntarily participate in the study and sign the informed consent.

Exclusion Criteria

  • Severe comorbidities, such as uncontrolled heart disease or diabetes History of major surgeries or other interventions Unwillingness to participate in the study

Outcomes

Primary Outcomes

Blood Loss

Time Frame: During the surgery

Assess the total blood loss during surgery in milliliters.

Postoperative Complications

Time Frame: Within 30 days post-surgery

Record any complications within 30 days post-surgery.

Operation Time

Time Frame: During the surgery

Measure the total duration of the surgery in minutes.

Study Sites (1)

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