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Prevention of Retinal Non-perfusion in Central Retinal Vein Occlusion by Hydroxycarbamide Treatment. (PNPRO_HC)

Primary Purpose

Central Retinal Vein Occlusion, Non-Ischemic

Status
Unknown status
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Hydroxycarbamid
Sponsored by
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Central Retinal Vein Occlusion, Non-Ischemic

Eligibility Criteria

45 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients of both sexes of at least 45 years of age.
  • with social protection
  • Presenting CRVO for less than 1 month duration
  • With a decrease of visual acuity and with the best corrected visual acuity lower than 6/10 (73 ETDRS letters)
  • Signature of informed consent

Exclusion Criteria:

  • predictable lack of compliance to the protocol
  • monophtalmic patient or any ocular history or condition that could interfere with the study course or results interpretation.
  • active systemic disease
  • sickle cell disease
  • myeloproliferative disease
  • myelosuppression
  • kidney or liver insufficiency
  • ongoing treatment with hydroxycarbamide or anticoagulant
  • Pregnancy, breast-feeding, no efficient contraception (for both sexes)
  • wish of paternity (for males of al least 45 years of age)

Sites / Locations

  • CHNO des Quinze-VingtsRecruiting

Outcomes

Primary Outcome Measures

retinal capillary non-perfusion
To assess the percentage of subjects in whom one of the following events will not be observed at W13 (any event being considered as one of the criteria of worsening of retinal capillary non-perfusion): Occurence of at least one direct sign of retinal ischemia: Increase of more than 30% of peripheral retinal non-perfusion on large-field angiography or of the central avascular zone of the retina, Occurence of at least one indirect sign of retinal ischemia: reperfusion of the aterial iris circle, rubeosis iridis, neovascular glaucoma or abolition of the afferent pupillary reflex.

Secondary Outcome Measures

retinal capillary non-perfusion
Same criteria of retinal non perfusion as for primary end point
Hydroxycarbamide safety - visual acuity and retinal thickness. Biological in vitro effects on erythrocyte adhesion to vascular endothelium and various haemorheological parameters.
HC effect on visual acuity and retinal thickness. Biological in vitro effects on erythrocyte adhesion to vascular endothelium and various haemorheological parameters.

Full Information

First Posted
November 4, 2016
Last Updated
November 25, 2016
Sponsor
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
Collaborators
Hopital Universitaire Robert-Debre, Institut National de la Transfusion Sanguine, Keyrus Biopharma, For Drug Consulting, ADDMEDICA SASA
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1. Study Identification

Unique Protocol Identification Number
NCT02957760
Brief Title
Prevention of Retinal Non-perfusion in Central Retinal Vein Occlusion by Hydroxycarbamide Treatment.
Acronym
PNPRO_HC
Official Title
Prevention of Retinal Non-perfusion in Central Retinal Vein Occlusion by Hydroxycarbamide Treatment.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Unknown status
Study Start Date
December 2015 (undefined)
Primary Completion Date
August 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
Collaborators
Hopital Universitaire Robert-Debre, Institut National de la Transfusion Sanguine, Keyrus Biopharma, For Drug Consulting, ADDMEDICA SASA

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The central retinal vein occlusion (CRVO) is a major cause of ocular morbidity, depending in particular on the occurrence and extent of retinal ischemia by capillary occlusion. There is no effective systemic treatment of this condition. An increase in the adhesion of erythrocytes to vascular endothelium was observed for patients with CRVO, correlated with overexpression of membrane phosphatidylserine
Detailed Description
introduction : The central retinal vein occlusion (CRVO) is a major cause of ocular morbidity, depending in particular on the occurrence and extent of retinal ischemia by capillary occlusion. There is no effective systemic treatment of this condition. An increase in the adhesion of erythrocytes to vascular endothelium was observed for patients with CRVO, correlated with overexpression of membrane phosphatidylserine. Hypothesis : Hydroxycarbamide (HC) by reducing the erythrocyte adhesion to the endothelium may prevent or delay the onset of retinal capillary non-perfusion in patients with CRVO. Primary objective: To assess the efficacy at 3 months of treatment with HC on retinal capillary perfusion in patients with a recent CRVO. Secondary Objectives: To evaluate the safety of the treatment, the efficacy to 6 months on retinal perfusion of the treatment with HC (HC peak effect on the red cell adhesion in vitro), and the biological effects of HC, in particular on adhesion to endothelium and erythrocyte hemorheological parameters.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Central Retinal Vein Occlusion, Non-Ischemic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Hydroxycarbamid
Other Intervention Name(s)
siklos
Intervention Description
20 mg/kg milligram(s)/kilogram per day during 6 month, oral administration (coated tablet).
Primary Outcome Measure Information:
Title
retinal capillary non-perfusion
Description
To assess the percentage of subjects in whom one of the following events will not be observed at W13 (any event being considered as one of the criteria of worsening of retinal capillary non-perfusion): Occurence of at least one direct sign of retinal ischemia: Increase of more than 30% of peripheral retinal non-perfusion on large-field angiography or of the central avascular zone of the retina, Occurence of at least one indirect sign of retinal ischemia: reperfusion of the aterial iris circle, rubeosis iridis, neovascular glaucoma or abolition of the afferent pupillary reflex.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
retinal capillary non-perfusion
Description
Same criteria of retinal non perfusion as for primary end point
Time Frame
2 weeks, 2 months and 6 months
Title
Hydroxycarbamide safety - visual acuity and retinal thickness. Biological in vitro effects on erythrocyte adhesion to vascular endothelium and various haemorheological parameters.
Description
HC effect on visual acuity and retinal thickness. Biological in vitro effects on erythrocyte adhesion to vascular endothelium and various haemorheological parameters.
Time Frame
2 weks, 2 months, 3 months and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients of both sexes of at least 45 years of age. with social protection Presenting CRVO for less than 1 month duration With a decrease of visual acuity and with the best corrected visual acuity lower than 6/10 (73 ETDRS letters) Signature of informed consent Exclusion Criteria: predictable lack of compliance to the protocol monophtalmic patient or any ocular history or condition that could interfere with the study course or results interpretation. active systemic disease sickle cell disease myeloproliferative disease myelosuppression kidney or liver insufficiency ongoing treatment with hydroxycarbamide or anticoagulant Pregnancy, breast-feeding, no efficient contraception (for both sexes) wish of paternity (for males of al least 45 years of age)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Laurent Vinet
Phone
+33140021126
Email
lvinet@15-20.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-François Girmens
Organizational Affiliation
CHNO des Quinze-Vingts
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHNO des Quinze-Vingts
City
Paris
ZIP/Postal Code
75012
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laurent Vinet
Phone
+33140021126
Email
lvinet@15-20.fr
First Name & Middle Initial & Last Name & Degree
Romain Duvernois
Phone
+33140021124
Email
rduvernois@15-20.fr

12. IPD Sharing Statement

Learn more about this trial

Prevention of Retinal Non-perfusion in Central Retinal Vein Occlusion by Hydroxycarbamide Treatment.

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