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Individualized En-DCR Augmented Reality Preoperative Quantitative Planning Method and System Based on Endoscopic Optical Axis Orthographic Projection and Three-Dimensional Anatomical Axial Distance Decoupling

Individualized En-DCR Augmented Reality Preoperative Quantitative Planning Method and System Based on Endoscopic Optical Axis Orthographic Projection and Three-Dimensional Anatomical Axial Distance Decoupling

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127902
Enrollment
Unknown
Registered
2026-07-09
Start date
2026-07-09
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Nasolacrimal duct obstruction-related disease, mainly including chronic dacryocystitis and epiphora

Interventions

Single-arm Observational Group:None

Sponsors

Eye Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Clinically diagnosed with nasolacrimal duct obstruction, chronic dacryocystitis, or other lacrimal drainage system disorders scheduled for En-DCR treatment; 2. Age 18 or older, any gender; 3. Completed preoperative thin-slice CT scans of the nasal cavity and tear ducts, with image quality sufficient for 3D reconstruction and measurements; 4. Able to cooperate in completing all data collection tasks for this study; 5. Voluntarily participating in this study and signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Poor CT image quality, making lacrimal sac segmentation, key anatomical landmark annotation, or subsequent measurement and analysis impossible; 2. Combined severe nasal cavity structural defects, large-scale space-occupying lesions, or significant anatomical abnormalities, where key anatomical landmarks cannot be identified; 3. Previous surgeries or injuries in the lacrimal duct area causing obvious local anatomical changes, making standardized data analysis impossible.

Design outcomes

Primary

MeasureTime frame
Consistency between preoperative quantitative planning and intraoperative anatomical exposure;

Secondary

MeasureTime frame
Generation of individualized preoperative planning images;Intra-observer repeatability and inter-observer agreement;Acquisition of quantitative parameters;

Countries

China

Contacts

Public ContactYikui Zhang

Eye Hospital, Wenzhou Medical University

zhang.yikui@wmu.edu.cn+86 577 88075582

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026