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临床试验/NCT03207100
NCT03207100已完成不适用

Clinical Study of the Safety and Efficacy of Analgesia-first Minimal Sedation as an Early Antihypertensive Treatment for Spontaneous Intracerebral Hemorrhage

Hong Yang17 个研究点 分布在 1 个国家目标入组 338 人开始时间: 2017年12月6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
发起方
入组人数
338
试验地点
17
主要终点
Systolic BP control rate at 1h post-treatment initiation

研究概览

简要总结

This study evaluates safety and efficacy of analgesia-first minimal sedation as an early antihypertensive treatment for spontaneous intracerebral hemorrhage. The analgesia-first minimal sedation strategy relies on the remifentanil-mediated alleviation of pain-induced stress response and the antisympathetic activity of dexmedetomidine to restore the elevated blood pressure to normal level in patients with spontaneous intracerebral hemorrhage. This strategy allows rapid stabilization of blood pressure, and its use as a pre-treatment for patients on mechanical ventilation prior to painful procedures reduces blood pressure variability and thereby results in etiologic treatment. It is more effective in blood pressure control than conventional symptomatic antihypertensive treatment, reduces the incidence of early hematoma expansion and improves prognosis, ,lowers healthcare workers workload, increases patient adherence, and improves healthcare worker satisfaction.

详细描述

Spontaneous intracerebral hemorrhage (ICH) is hemorrhage in the brain parenchyma caused by non-traumatic spontaneous rupture of cerebral artery, arteriole, vein and capillary in adults. ICH is a common problem, with subarachnoid hemorrhage. About 90% ICH patients have increased blood pressure (BP) that usually occurs immediately after disease onset. BP elevation in the acute phase of ICH is associated with poor prognosis, and its mechanism of action includes the local increase of initial hemorrhage, early hematoma expansion at hemorrhagic sites, the increased risk of early recurrent hemorrhage, serious cerebral edema, and recurrent stroke, this affects the most within the few hours following the onset of the disease. The current American Heart Association guidelines recommended early antihypertensive treatment and suggested that rapid decrease of BP to 140 mmHg is safe in ICH patients with no obvious antihypertensive contraindications. However, the significant differences between large studies conducted in recent years have led to great controversy on the effect of early antihypertensive treatment in acute ICH and disease prognosis. A meta-analysis of early antihypertensive treatment for ICH showed that differences in early BP control rate and BP increase variability are also the major causes of inconsistency between these studies. There is currently no consensus on the best antihypertensive regimen as it is difficult to reach the optimal BP level timely. Some studies have shown that stress response, pain, ICP increase and pre-onset BP elevation are factors that cause acute BP increase in ICH patients. In particular, restlessness, sleep deprivation, and stress due to intolerable pain can lead to dramatic BP and intracranial pressure (ICP) increases, further lead to secondary intracerebral hematoma expansion and subsequently cause neurologic degeneration and cerebral tissue damage. Therefore, the primary principles of ICH acute BP increase treatment are to keep quiet, restore BP to normal level, stably reduce BP, decrease BP variability, lower the chance of recurrent hemorrhage, and thereby improve long-term prognosis. Traditional antihypertensive treatment can only resolve the issue of BP elevation but not the root cause of disease. Analgesia and sedation is a critical component of and a global consensus in the clinical management of ICH patients. Remifentanil is a fentanyl μ-type opioid receptor agonist with strong and fast-acting analgesic effects, does not induce ICP elevation and can alleviate pain induced by sputum aspiration, body turning and back clapping in severe patients. A randomized trial on patients with craniocerebral injury has indicated that a remifentanil-based sedation strategy can significantly reduce the amount of sedative used and shorten the time of mechanical ventilation without affecting the functional assessment of the nervous system. Dexmedetomidine is an α2-adrenergic agonist that inhibits sympathetic activity by activating the pre-synaptic α2-receptor in the locus coeruleus, which in turn reduces norepinephrine release, that only slightly affects consciousness and breathing and helps patients with craniocerebral injury stay conscious while under sedation, allowing real-time functional assessment of the nervous system. Therefore, the research group developed a treatment strategy in which sufficient analgesia is applied in combination with a minimal sedation program as an effective and safe early an- tihypertensive treatment.We hypothesize that applying sufficient analgesia in combination with a minimal sedation program will involve the use of remifentanil for pain relief and dexmedetomidine for antisympathetic activity to restore elevated BP to normal levels in patients with spontaneous ICH, and we further hypothesize that this strategy will be more effective than conventional symptomatic antihypertensive treatment for controlling BP.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

盲法说明

This study uses a single-blinded design in which only the investigators and not the subjects know the method of intervention.

入排标准

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

入选标准

  • •Definitive diagnosis of ICH-induced acute brain injury by CT;
  • •Systolic BP ≥150 mmHg for at least twice;
  • •>18 years old;
  • •Feasible for emergency antihypertensive treatment and real-time BP monitoring;
  • •Disease onset is within 24h;
  • •ICU or stroke unit admission within 24h.

排除标准

  • •Subject has contraindications for emergency intensified antihypertensive treatment;
  • •Intracranial hemorrhage secondary to intracranial tumor, recent trauma, cerebral infarction and thrombolytic therapy;
  • •History of ischemic stroke within 30 days before disease onset;
  • •Clinical or imaging examination reveals an expected high mortality in subject within the next 24h;
  • •Presence of dementia or significant post-stroke disability;
  • •Coagulation disorder caused by drugs or hematologic diseases;
  • •Allergy to opioids;
  • •Interference test result, assessment and follow-up of comorbidity;
  • •Presence of sinus arrest, borderline rhythm, grade II and above atrioventricular block and malignant arrhythmia;
  • •Individual is pregnant or lactating;
  • •Currently participating in other drug studies or clinical trials;
  • •Subject or guardian is unwilling to provide his/her informed consent form, or subject is highly unable to persist with the study and follow-up;
  • •Subject's participation in the study will increase his/her study-related risk, and other reasons that make the subject unsuitable for the study as determined by the investigator.

研究组 & 干预措施

Analgesia-first minimal sedation group

Experimental

Using analgesia-first minimal sedation strategy to implement antihypertensive therapy.

干预措施: Analgesia-first minimal sedation (Combination Product)

Antihypertensive drug treatment group

Active Comparator

Using routine antihypertensive drugs to implement antihypertensive therapy.

干预措施: Antihypertensive treatment (Combination Product)

结局指标

主要结局

Systolic BP control rate at 1h post-treatment initiation

时间窗: 1h post-treatment initiation

The number of patients who systolic BP decreased to \<140 mmHg at 1h post-treatment initiation compared to the total number of each group.

次要结局

  • Hematoma growth at 24 h(24h of treatment)
  • Healthcare worker satisfaction(7 day or discharge from ICU (if patients discharge from ICU in 7 days))
  • 28-day mortality and disability rate(28 days)
  • 90-day mortality and disability rate(90 days)
  • BP variability(Up to 7 days)
  • Duration of ICU treatment and mechanical ventilation(Up to 7 days)
  • cerebral tissue oxygenation index (TOI)(Up to 7 days and around sputum aspiration)
  • Neurologic function(Up to 7 days)

研究者

发起方
Hong Yang
申办方类型
Other Gov
责任方
Sponsor Investigator
主要研究者

Hong Yang

Doctor of Medicine (M.D.);Associate Senior Doctor

The Third Affiliated Hospital of Southern Medical University

研究点 (17)

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