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临床试验/NCT02557451
NCT02557451已完成不适用

Subretinal Haematoma in AMD: Randomized Controlled Study of 2 Therapeutic Approaches in the Antiangiogenic Era

Centre Hospitalier Universitaire Dijon17 个研究点 分布在 1 个国家目标入组 91 人开始时间: 2016年4月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
91
试验地点
17
主要终点
Visual acuity measured on the ETDRS scale

研究概览

简要总结

AMD is a disease of the central retina, a zone that enables fine detail activities (reading, detail…). This central zone of the retina can be affected by a haemorrhagic complication when small abnormal vessels suddenly start to bleed inside the retina. Several therapeutic approaches are currently available even though they have never been truly compared. The study will be proposed to patients who need to be treated for haemorrhage of the macula. A certain number of factors will be evaluated to compare the 2 principal approaches currently used in France: surgery followed by injections of an anti-angiogenic OR intravitreal injections of gas followed by injections of anti-angiogenics. This is a multicentre, randomized controlled trial to compare these 2 therapeutic approaches.

These diametrically opposed approaches have very different consequences for patients and in terms of cost for society. The consequences for patients will be immediately measurable so as to determine the best therapeutic approach in terms of functional recovery and the impact of the disease on quality of life, while taking into account the risks inherent to these 2 treatments. The impact on quality of life of these 2 approaches as well as their consequences - an important factor in this disease, which is a cause of sensory handicap - will provide the ophthalmological community with essential information making it possible to validate one or the other of these methods for the management of these haematomas.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
None

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients presenting subretinal haematoma linked to AMD
  • Occurring at least14 days before the start of therapy
  • With the presence of a component overlying the pigmentary epithelium (PE) on the OCT
  • And a diameter greater than two pupillary diameters on the retinal photographs
  • Patients who have provided oral consent
  • Patients with National Health Insurance cover
  • Patients available for monthly follow-up
  • Patient having an effective contraception for the women old enough to procreate during the treatment and during 6 months which follow his stop.

排除标准

  • Subretinal haematoma linked to a cause other than AMD (myopia, angioid streaks…)
  • History of subretinal haematoma on the same side
  • Cloudy humour making it impossible to photograph the fundus of the eye or carry out angiography
  • Component of the haematoma exclusively underlying the pigmentry epithelium
  • Haemorrhage without lifting of the retina
  • Patients presenting an INR greater than 4, thus contra-indicating surgery
  • Patients requiring cataract surgery in the first 3 months of the study
  • Patients presenting a contra-indication relative to injection of the antiangiogenic (History of AVC bleeding or unknown origin in the last 6 months or MI in the 3 preceding months)
  • Pregnant or breast-feeding woman (the patients do not have to breast-feed during at least 6 months after the administration of the last dose of the antiangiogénique)
  • Contraindication in the use of ranibizumab: hypersensitivity in the active ingredient or in one of the excipients, eye infection or périoculaire active or suspected, inflammation intraoculaire active severe, treatments anti-VEGF systematic or eye concomitant,
  • Contraindication in the use of bevacizumab: hypersensitivity in the active substance or in one of the excipients, the hypersensitivity in the products of the ovarian cells of Chinese hamster (CHO) or in other antibodies human or humanized recombinants, heavy surgical operation dating less than 28 days, not totally healed surgical wound, history of lung bleeding or hémoptysie
  • Contraindication in the use of alteplase: hypersensitivity in the active substance, in the gentamicine (a residue of the present manufacturing process in the state of tracks), or in one of the excipients. As all the thrombolytic agents, contraindication in every case associated to a high hemorrhagic risk (current significant hemorrhagic disorder or during the last six months, hemorrhagic known diathesis, concomitant treatment by oral anticoagulants with effective dose, severe or potentially dangerous, obvious or recent bleeding, histories or suspicion of intra-cranial bleeding, suspicion of sub-arachnoid bleeding or history of sub-arachnoid bleeding bound to an aneurysm, histories of severe lesion of the central nervous system (for example néoplasie, aneurysm, surgical operation intracerebral or intrathecal), recent traumatic external cardiac massage (less than 10 days), delivery, recent draining of a vessel not accessible to the compression (for example draining of the subclavian or jugular vein),severe uncontrolled high blood pressure, bacterial endocarditis, pericarditis, acute pancreatitis, gastrointestinal ulcers documented during the last 3 months, esophageal varices, arterial aneurysm, arterial or venous deformations, neoplasia increasing the hemorrhagic risk, severe hepatic disease, including hepatic insufficiency, cirrhosis, portal hypertension (esophageal varicose veins) and evolutionary hepatitis, surgical operation or important traumas during the last 3 months.
  • Contraindication in the use of acetazolamide: hypersensitivity in the acetazolamide or in one of excipients, severe hepatic, renal or suprarenal inadequacies, intolerance in sulphonamide, histories of renal colic, allergy in the wheat (other than the coeliac disease).

研究组 & 干预措施

intravitreal injection of gas/TPA + antiangiogenic

Experimental

intravitreal injection of gas - TPA with injections of an antiangiogenic

干预措施: Intravitreal injections of gas (Other)

intravitreal injection of gas/TPA + antiangiogenic

Experimental

intravitreal injection of gas - TPA with injections of an antiangiogenic

干预措施: injections of an antiangiogenic (Procedure)

surgery + antiangiogenic

Experimental

surgery (vitrectomy - air - TPA) with injections of an antiangiogenic

干预措施: Surgery (Other)

surgery + antiangiogenic

Experimental

surgery (vitrectomy - air - TPA) with injections of an antiangiogenic

干预措施: injections of an antiangiogenic (Procedure)

结局指标

主要结局

Visual acuity measured on the ETDRS scale

时间窗: Change from inclusion at 3 months

次要结局

  • Area of the scotoma presented by the patient according to the Amsler grid(At 1 month, 3 months and 6 months)
  • Complications rate(At 6 months)
  • Visual acuity measured on the ETDRS scale(At 1 month and 6 months)
  • Quality of life using the VFQ-25 scale(At 3 months and 6 months)
  • Number of injections of an antiangiogenic at the end of the 6 months of treatment(At 6 months)
  • Area of hypoautofluorescence using the autofluorescence technique(At 3 and 6 months)
  • Number of patients with macular bleeding(At 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (17)

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