Safety and Efficacy After Selective Intra-arterial Thrombolysis for Central Retinal Artery Occlusion

Sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine (Other)
Overall Status
Recruiting
CT.gov ID
NCT05562284
Collaborator
(none)
128
1
2
22
5.8

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: intra-arterial thrombolysis
  • Other: conservative treatments
N/A

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. Thus, IAT 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. Sequential evaluation by Humphrey perimetry will evaluate the temporal changes before and after IAT or conservative therapies. Our study will enroll patients within 7 days of symptom onset and aims at evaluating the safety of IAT and comparing the improvement of the VFDs between conservative treatments and IAT combined with conservative treatments.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
128 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Safety and Efficacy of the Visual Field Improvement After Selective Intra-arterial Thrombolysis for Central Retinal Artery Occlusion
Actual Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
Mar 31, 2024
Anticipated Study Completion Date :
Mar 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: IAT combined with conservative therapies

IAT (Drug: 50 mg Alteplase)+conservative treatments

Procedure: intra-arterial thrombolysis
IAT introduces rt-PA directly into the ophthalmic circulation by super-selective microcatheterization.

Other: conservative treatments
conservative treatments

Other: Conservative therapies

conservative treatments including traditional ones and hyperbaric oxygen therapy

Other: conservative treatments
conservative treatments

Outcome Measures

Primary Outcome Measures

  1. Change of the visual field index as mean deviation (MD) examed by Humphrey visual field analyzer at 3 months [90 days]

    Change of the mean deviation

  2. Change of the visual field index as visual field index (VFI) examed by Humphrey visual field analyzer at 3 months [90 days]

    Change of the visual field index

Secondary Outcome Measures

  1. Change of Best corrected visual acuity (BCVA) at 3 months [90 days]

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

  2. Adverse reactions at 1 month [30 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:
Yes
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,

  4. Meet the inclusion of HBOT

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 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:
NCT05562284
Other Study ID Numbers:
  • XHEC-C-2022-056
First Posted:
Sep 30, 2022
Last Update Posted:
Sep 30, 2022
Last Verified:
Sep 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Ping Fei, Associate professor, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 30, 2022