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Efficacy evaluation research of endoscopic endonasal optic nerve decompression for cranial fibrous dysplasia in adolescents

Efficacy evaluation research of endoscopic endonasal optic nerve decompression for cranial fibrous dysplasia in adolescents

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055926
Enrollment
Unknown
Registered
2022-01-25
Start date
2020-06-01
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

cranial fibrous dysplasia

Interventions

EEA treatment group:None
MCA treatment group:None

Sponsors

Beijing Tongren Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Aged 6 to 18 years, male or female; 2.Imaging examination: CT diagnosis of craniofacial fibrous dysplasia, the lesions oppress the orbital apex and optic canal; 3.The uncorrected visual acuity decreased and the visual acuity of the affected eye was less than 0.5; 4.Informed consent signed by guardian.

Exclusion criteria

Exclusion criteria: 1. Other diseases are known to cause vision loss or visual field defect; 2. Unable to cooperate with visual examination due to brain or mental illness; 3. Before the start of this study, surgery, radiotherapy and drug therapy were given; 4. Other conditions are not suitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
Visual acuity;Dynamic vision;Retinal nerve fiber layer thickness;

Countries

China

Contacts

Public ContactKang Jun

Beijing Tongren Hospital, Capital Medical University

junkang2015@163.com+86 13901038977

Outcome results

None listed

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