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Phase I RVC With Ocriplasmin for CRVO (RVC_CRVO)

Primary Purpose

Central Retinal Vein Occlusion

Status
Completed
Phase
Phase 1
Locations
Belgium
Study Type
Interventional
Intervention
Ocriplasmin intravenously
Sponsored by
Universitaire Ziekenhuizen KU Leuven
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Central Retinal Vein Occlusion focused on measuring Central retinal vein occlusion, Retinal endovascular surgery, Retinal vein cannulation, Ocriplasmin

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients aged over 18 years
  • Recent diagnosis of CRVO
  • Onset of symptoms <10 days
  • Visual acuity < 2/10 in study eye
  • Visual acuity >1/10 in fellow eye
  • Central macular thickness >250µm and <1000 µm
  • Signed informed consent prior to inclusion

Exclusion Criteria:

  • Fluorescein allergy
  • Active neovascularization (NVD/NVE/NVI/NVA)
  • Eye disease other than CRVO or Cataract decreasing vision
  • Use of acetazolamide or other drugs potentially affecting macular edema, including systemic steroids >10mg/d
  • History of retinal surgery
  • High myopia (> -10D)
  • Contraindication for the use of systemic anticoagulant medication

Sites / Locations

  • UZ Leuven

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Ocriplasmin intravenously

Arm Description

All subjects included in this phase I study are in the experimental treatment arm and will undergo a vitrectomy augmented with retinal vein cannulation and intravenous Ocriplasmin infusion.

Outcomes

Primary Outcome Measures

Feasibility
technical succes of retinal vein cannulation and duration of infusion time
Safety
number of intervention-related (surgical or pharmacological) complications

Secondary Outcome Measures

central macular thickness
change in central macular thickness as measured with optical coherence tomography
surface of non-perfused retina
change in surface of non-perfused retina as measured with fluo-angiography
visual acuity
change in visual acuity

Full Information

First Posted
April 18, 2016
Last Updated
January 4, 2018
Sponsor
Universitaire Ziekenhuizen KU Leuven
Collaborators
KU Leuven
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1. Study Identification

Unique Protocol Identification Number
NCT02747030
Brief Title
Phase I RVC With Ocriplasmin for CRVO
Acronym
RVC_CRVO
Official Title
Phase I Study on the Feasibility and Safety of Surgical Stabilizer Assisted Retinal Vein Cannulation With Ocriplasmin Infusion for Central Retinal Vein Occlusion.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
December 2016 (undefined)
Primary Completion Date
August 10, 2017 (Actual)
Study Completion Date
August 11, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitaire Ziekenhuizen KU Leuven
Collaborators
KU Leuven

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In central retinal vein occlusion (CRVO) a blood clot blocks the venous outflow of the entire retinal circulation. This leads to retinal and vitreous hemorrhages, retinal edema and neovascularization. The development of a microneedle and surgical stabilizer made it possible to perform a prolonged (10 minutes) retinal vein cannulation with infusion of Ocriplasmin. Ocriplasmin has the advantage over tissue Plasminogen Activator (tPA) that it already is an active enzyme and a strong fibrinolyticum. This study aims to investigate the feasibility and safety of local intravenous Ocriplasmin for CRVO.
Detailed Description
Central retinal vein occlusion (CRVO) is the second most common source of permanent blindness in the Western world after diabetic retinopathy. By blocking the outflow pathway for the retinal circulation, visual prognosis is bad on the short and long term. Currently, treatment is mostly focused on treating the secondary effects: macular edema and neovascularization with antiVEGF and/or corticosteroid intravitreal injections and retinal laser photocoagulation. There is however a surgical treatment aimed at displacing the blood clot; a radial optic neurotomy. During this surgical treatment, the vitreous is removed by vitrectomy, after which a radial incision is made in the optic disc. The target of this incision is to open the canal in the lamina cribrosa to improve the blood flow in the central retinal vein. Since the outcome of this procedure is variable and has its inherent risks, mainly because the incision can damage the central retinal artery which is adjacent to the central vein, this procedure is not routinely performed in all vitreoretinal centers. Following the recent development of a surgical stabilizer and microneedle suitable for retinal vein cannulations, the option for local intravenous administration of fibrinolytic drugs exists. This phase I study aims to investigate the feasibility and safety of surgical stabilizer assisted retinal vein cannulation with local intravenous infusion of Ocriplasmin to dissolve the clot clogging the central retinal vein. Ocriplasmin is the small active part of the larger plasmin molecule. Plasmin itself is formed by enzymatic conversion from plasminogen, a process that is mediated by tissue plasminogen activator (tPA). The amount of plasmin that can be produced is thus highly dependent on the amount of plasminogen that is present nearby the clot. By using Ocriplasmin, this intermediate step can be skipped and the clot will be targeted directly and during the entire time of infusion. By being able to get infusion times up to 10 minutes, abundant clot exposure to Ocriplasmin is guaranteed. Inclusion will be offered to patients presenting with a recent CRVO, a vitrectomy will be performed augmented with retinal vein cannulation and infusion of ocriplasmin during 10 minutes. Patients presenting with a recent CRVO (<2weeks) will be offered inclusion to undergo a vitrectomy with subsequent prolonged retinal vein cannulation and infusion of Ocirplasmin. The surgery is done by placing a microneedle in one of the branch retinal veins at the border of the optic disc. To increase the safety of this procedure a surgical stabilizer was developed. This procedure was abundantly tested and refined in multiple in vivo porcine experiments and the medication (Ocriplasmin) has already been tested for fibrinolytic activity used in 100-fold higher dosis intravenously and intra-arterially. After the surgery, standard of care follow up with a comprehensive ophthalmological examination and technical investigations is foreseen. The primary outcome measures of this safety and feasiblity study are: technical success to cannulate the retinal vein and inject ocriplasmin to remove the blood clot, number of intervention-related (surgical or pharmacological) complications, duration of infusion. If necessary; depending on the disease evolution, additional interventions like intravitreal antiVEGF, steroids or laser photocoagulation can be performed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Central Retinal Vein Occlusion
Keywords
Central retinal vein occlusion, Retinal endovascular surgery, Retinal vein cannulation, Ocriplasmin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
4 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ocriplasmin intravenously
Arm Type
Experimental
Arm Description
All subjects included in this phase I study are in the experimental treatment arm and will undergo a vitrectomy augmented with retinal vein cannulation and intravenous Ocriplasmin infusion.
Intervention Type
Drug
Intervention Name(s)
Ocriplasmin intravenously
Other Intervention Name(s)
Jetrea
Intervention Description
Retinal vein cannulation with Ocriplasmin infusion
Primary Outcome Measure Information:
Title
Feasibility
Description
technical succes of retinal vein cannulation and duration of infusion time
Time Frame
peroperative
Title
Safety
Description
number of intervention-related (surgical or pharmacological) complications
Time Frame
peroperative until 2 weeks postoperative
Secondary Outcome Measure Information:
Title
central macular thickness
Description
change in central macular thickness as measured with optical coherence tomography
Time Frame
2 weeks
Title
surface of non-perfused retina
Description
change in surface of non-perfused retina as measured with fluo-angiography
Time Frame
2 weeks
Title
visual acuity
Description
change in visual acuity
Time Frame
2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged over 18 years Recent diagnosis of CRVO Onset of symptoms <10 days Visual acuity < 2/10 in study eye Visual acuity >1/10 in fellow eye Central macular thickness >250µm and <1000 µm Signed informed consent prior to inclusion Exclusion Criteria: Fluorescein allergy Active neovascularization (NVD/NVE/NVI/NVA) Eye disease other than CRVO or Cataract decreasing vision Use of acetazolamide or other drugs potentially affecting macular edema, including systemic steroids >10mg/d History of retinal surgery High myopia (> -10D) Contraindication for the use of systemic anticoagulant medication
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Stalmans, MD PhD
Organizational Affiliation
UZ Leuven
Official's Role
Principal Investigator
Facility Information:
Facility Name
UZ Leuven
City
Leuven
State/Province
Vlaams Brabant
ZIP/Postal Code
3000
Country
Belgium

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26310993
Citation
van Overdam KA, Missotten T, Spielberg LH. Updated cannulation technique for tissue plasminogen activator injection into peripapillary retinal vein for central retinal vein occlusion. Acta Ophthalmol. 2015 Dec;93(8):739-44. doi: 10.1111/aos.12830. Epub 2015 Aug 27.
Results Reference
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PubMed Identifier
22634985
Citation
Verhamme P, Heye S, Peerlinck K, Cahillane G, Tangelder M, Fourneau I, Daenens K, Belmans A, Pakola S, Verhaeghe R, Maleux G. Catheter-directed thrombolysis with microplasmin for acute peripheral arterial occlusion (PAO): an exploratory study. Int Angiol. 2012 Jun;31(3):289-96.
Results Reference
background
PubMed Identifier
19834019
Citation
Thijs VN, Peeters A, Vosko M, Aichner F, Schellinger PD, Schneider D, Neumann-Haefelin T, Rother J, Davalos A, Wahlgren N, Verhamme P. Randomized, placebo-controlled, dose-ranging clinical trial of intravenous microplasmin in patients with acute ischemic stroke. Stroke. 2009 Dec;40(12):3789-95. doi: 10.1161/STROKEAHA.109.560201. Epub 2009 Oct 15.
Results Reference
background
PubMed Identifier
19225865
Citation
Verhamme P, Jerome M, Goossens G, Devis J, Maleux G, Stas M. A pilot trial of microplasmin in patients with long-term venous access catheter thrombosis. J Thromb Thrombolysis. 2009 Nov;28(4):477-81. doi: 10.1007/s11239-009-0310-x. Epub 2009 Feb 19.
Results Reference
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Phase I RVC With Ocriplasmin for CRVO

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