Changes of Visual Field Defects After IAT for CRAO

Sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine (Other)
Overall Status
Completed
CT.gov ID
NCT05739487
Collaborator
(none)
27
1
21
1.3

Study Details

Study Description

Brief Summary

Central retinal artery occlusion (CRAO) is an ophthalmic emergency which leads to devastating visual function defects and poor prognosis. Though traditional conservative treatments are widely used, none of them is proved to be effective. A number of meta-analyses and observational studies indicate intravenous thrombolysis to be beneficial in CRAO. Selective intra-arterial thrombolysis (IAT) introducing rt-PA directly into the ophthalmic circulation by super-selective microcatheterization may reduce the complications such as intracranial and systemic hemorrhage. The residual visual field is significant for patients with CRAO who have poor central visual acuity. Thus, it is clinically significant to study the changes in visual fields in eyes with CRAO.

Condition or Disease Intervention/Treatment Phase
  • Procedure: selective intra-arterial thrombolysis

Detailed Description

Central retinal artery occlusion (CRAO) is an ophthalmic emergency which leads to devastating visual function defects and poor prognosis. Though traditional conservative treatments are widely used, none of them is proved to be effective. The respective responses of brain and retinal tissues to acute ischemia share many features is the rationale for therapeutic thrombolysis in CRAO. Intravenous thrombolysis (IVT) has been a therapeutic choice for CRAO since the 1960s, and in the United States, tPA is currently administered in 5.8% of patients admitted with CRAO. A number of meta-analyses and observational studies indicate intravenous thrombolysis to be beneficial in CRAO. Selective intra-arterial thrombolysis (IAT) introducing rt-PA directly into the ophthalmic circulation by super-selective microcatheterization which has the advantage of reducing the dose of rt-PA reaching the systemic circulation. It is clinically significant to study the changes in visual fields in eyes with CRAO. The short-term temporal changes (≤7-day) of VFDs and the adverse reactions in eyes with CRAO after IAT were investigated to assess the efficacy and safety of the procedure in this retrospective study.

Study Design

Study Type:
Observational
Actual Enrollment :
27 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Changes of Visual Field Defects After Selective Intra-arterial Thrombolysis for Central Retinal Artery Occlusion
Actual Study Start Date :
Jul 1, 2020
Actual Primary Completion Date :
Mar 31, 2022
Actual Study Completion Date :
Mar 31, 2022

Arms and Interventions

Arm Intervention/Treatment
IAT therapy

patients with central retinal artery occlusion received selective intra-arterial thrombolysis

Procedure: selective intra-arterial thrombolysis
IAT introduces rt-PA (50mg) directly into the ophthalmic circulation by super-selective microcatheterization

Outcome Measures

Primary Outcome Measures

  1. Change of the mean deviation [7 days]

    Change of the visual field index as mean deviation (MD) examed by Humphrey visual field analyzer at 7days

  2. Change of the visual field index [7 days]

    Change of the visual field index as visual field index (VFI) examed by Humphrey visual field analyzer at 7 days

Secondary Outcome Measures

  1. Change of best corrected visual acuity (BCVA) [7 days]

    best corrected visual acuity of logarithm of the minimum angle of resolution

  2. Adverse reactions at 7 days [7 days]

    Death, symptomatic or asymptomatic intracranial hemorrhage, intraocular hemorrhage

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
    1. Non-arteritic CRAO with symptom duration ≤7d 2. Age from 18 years old between 80 years old 3. Qualified systemic conditions, well-controlled blood pressure, well-controlled blood glucose, qualified liver and kidney function, no allergic history to contrast agent or rt-PA.
Exclusion Criteria:
  • Ocular factor or disease
  1. Branch retinal artery occlusion

  2. Combined retinal vein occlusion

  3. Suspicious ocular ischemic syndrome, such as ophthalmic artery occlusion or carotid artery occlusion

  4. Existed retinal problems decreasing visual function, such as macular disease, severe nonproliferative or proliferative diabetic retinopathy, severe cataract or glaucoma

  5. Central retinal artery occlusion from iatrogenic cause

  6. History of thrombolysis for CRAO or CRVO

  • Systemic factors restricting thrombolysis
  1. Uncontrolled hypertension (systolic blood pressure > 180mmHg ); Uncontrolled hyperglycemia (fasting blood glucose > 9mmol/L);

  2. Coagulation disorder

  3. History of intracranial hemorrhage, heart attack, cerebral infarction, or intracranial surgery within 3 mo

  4. Current antithrombotic treatment

  5. History of allergic reaction to contrast agent or rt-PA

Contacts and Locations

Locations

Site City State Country Postal Code
1 Xinhua Hospital, Shanghai Jiao Tong University School of Medicine Shanghai Shanghai China 200092

Sponsors and Collaborators

  • Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Investigators

  • Principal Investigator: Ping Fei, MD#PhD, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ping Fei, Associate professor, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
ClinicalTrials.gov Identifier:
NCT05739487
Other Study ID Numbers:
  • XHEC-C-2022-057-1
First Posted:
Feb 22, 2023
Last Update Posted:
Feb 22, 2023
Last Verified:
Feb 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 22, 2023