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临床试验/NCT04031508
NCT04031508Enrolling By Invitation2 期

Effect of a Parenteral Emulsion With LC-PUFA Omega 3 on Clinical Outcomes, Inflammatory and Oxidative Stress Markers in Neonates With Persistent Pulmonary Hypertension Associated With Congenital Diaphragmatic Hernia

Coordinación de Investigación en Salud, Mexico1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2019年8月12日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
Enrolling By Invitation
发起方
入组人数
40
试验地点
1
主要终点
Inspired fraction of oxygen (FiO2)

研究概览

简要总结

The purpose of this study is to evaluate the effect of a parenteral emulsion containing n-3 long-chain polyunsaturated fatty acids (LC-PUFA) in fish oil on clinical outcomes, markers of inflammation and oxidative stress, and pain in neonates with persistent pulmonary hypertension of the newborn (PPHN) compared with those who receive an emulsion containing soy oil and medium-chain triglycerides (MCT) without n-3 LC-PUFA.

详细描述

Background. Persistent pulmonary hypertension of the newborn (PPHN), is a syndrome characterized by difficulty to provide normal pulmonary vasodilatation at birth or after birth, which may be related to right ventricular dysfunction, congenital diaphragmatic hernia, sepsis, and meconium aspiration. This condition is understudied. PPHN causes pulmonary vascular resistance (PVR) that decreases left pulmonary artery flow (LPA), meaning that blood cannot be oxygenated in the lungs, leading to low oxygen delivery to all organs. Expensive medication along with ventilator support may help, but the latter and PPHN increase the production of the inflammatory mediators such as pro-inflammatory cytokines and markers of oxidative stress, which cause cell toxicity. To treat the hernia, infants undergo corrective surgery, which further increases the production of inflammatory markers and worsens oxidative stress. As a result, the pain of the surgery also worsens the hypoxemia and respiratory insufficiency in the newborn. PPHN is associated with chronic lung disease (CLD). To date, there is no effective treatment for neonates with PPHN, and around one-third of patients may not respond to current management, leading to the death of up to 33% of infants in developed countries. In Mexico, the mortality rate from PPHN may reach 80%, which is an unacceptable outcome at a high cost. Therefore, the prevention or reduction of the severity of PPHN is actively sought.

Previous reports have shown that the n-3 long-chain polyunsaturated fatty acids (LC-PUFA), such as docosahexaenoic acid (DHA) improves the nutritional status and clinical outcomes in septic newborn reduce systemic inflammation and organ dysfunction in newborns who underwent cardiovascular surgery with a shorter stay in the neonatal intensive care unit. In addition, those babies received lower amounts of analgesics. Other authors have shown that n-3 LC-PUFA reduces oxidative stress. In experimental models of PPHN, the EPA and DHA from Omegaven (fish oil) increased pulmonary artery flow and decrease pulmonary vascular resistance. In the current project, it is hypothesized that n-3 LC-PUFA improves clinical outcomes such as decreasing pulmonary vascular pressure and markers of inflammation and oxidative stress in neonates with PPHN. This hypothesis has not been evaluated.

Objective. The purpose of this study is to evaluate the effect of a parenteral emulsion containing n-3 LC-PUFA in fish oil on clinical outcomes, markers of inflammation and oxidative stress, and pain in neonates with PPHN compared with those who receive an emulsion containing soy and medium-chain triglycerides (MCT) without n-3 LC-PUFA.

Methodology. A double-blind clinical trial will be carried out on Mexican newborns diagnosed with PPHN. The control group will receive intravenous nutrition support including a lipid emulsion based on soy oil plus MCT (control group) and the intervention group will receive a lipid emulsion based on soy oil, MCT, olive oil, and fish oil (n-3 LC-PUFA group); both groups will receive a dose of lipid (3 g/kg/d maximum), through total parenteral nutrition (TPN) for at least 7 days.

The effect of n-3 LC-PUFA will be evaluated on:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

盲法说明

The attendant gastroenterologist has a randomized allocation and will indicate the type of emulsion during the recruitment. Each emulsion will be designed as a code A or B. The code for each patient is stored into an opaque envelop, which is opened once the parents have given their written informed consent.

入排标准

年龄范围
1 Hour 至 15 Days(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Plan to administrate TPN for at least 7 days
  • •Clinical, gasometric, and echocardiographic diagnosis of congenital diaphragmatic hernia.
  • •Gestational age >=34 weeks.
  • •Written informed consent signed by both parents after an explanation of the objectives, procedures and possible risks and benefits of the research, along with the signature of two witnesses

排除标准

  • •Diagnosis of complex congenital cardiopathy
  • •Cyanotic congenital cardiology defect
  • •Insufficiency of the tricuspid valve
  • •Immunosuppressive disease. HIV has been associated with PPHN and human herpesvirus with vascular remodeling, perivascular macrophages, and lung fibrosis
  • •Clinical entities that preclude the total parenteral nutrition for one day or longer.
  • •Presence of profuse and persistent haemorrhage at any level
  • •Elimination criteria
  • •Parents who withdraw their consent.
  • •Starting a drug at doses for nonclotting treatment such as heparin, enoxaparin.
  • •Development of profuse and persistent haemorrhage at any level after receiving vitamin K treatment.

研究组 & 干预措施

Omega 3

Experimental

The experimental group will receive a parenteral emulsion containing soy oil, MCT, olive oil and n-3 LCPUFA in fish oil

干预措施: lipid injectable emulsion with Fish oil (Combination Product)

Control group

Sham Comparator

The Control group will receive a parenteral emulsion containing soy oil and MCT

干预措施: lipid injectable emulsion with Fish oil (Combination Product)

结局指标

主要结局

Inspired fraction of oxygen (FiO2)

时间窗: Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.

Oxygen concentration supplied by ventilation support in percentage

Preductal partial pressure of carbon (PaCO2)

时间窗: Before surgery (baseline), 24 hour, 48 hour, 72 hour and day 7 post-surgery.

Good response if the carbon in blood is \<60-70 mmHg measured by gasometry in arterial blood

Pain manifestation

时间窗: Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.

Pain will be measured with the COMFORT scale computed by eight sections with scores from 1 to 5 each.

Change on systolic pressure of pulmonary artery

时间窗: Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.

Measured by echocardiography in millimeters of mercury (mm/Hg)

Change in Preductal and postductal oxygen saturation (SatO2)

时间窗: Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.

It is a measure of oxygenation in hemoglobin. It is preductal if the measurement id on hand, and postductal if it is on foot, determined by an pulse oximeter in percentage

Growth velocity and Nutritional status

时间窗: Before surgery (baseline), day 7, day 14 and day 21 post-surgery.

Measurement of body weight in grams, length, and head circumference in centimeters (if clinical condition allows it) to obtain grams/kg/d, cm/week, Z score, and eutrophic or undernutrition outcome using the Fenton's standard reference of growth and/or World Health Organization as appropriate for preterm or term infants, respectively.

次要结局

  • Concentration of the nuclear factor erythroid 2-related factor 2 (Nrf2)(At study entry, before surgery (2 baselines), and once a day until day 7 after surgery, then at 14 and 21 days-post-surgery.)
  • Chronic Lung Disease(At hospital discharge or 56 day-old, at 6 months and one year of age)
  • Concentration of plasma cytokines as inflammatory markers(Before surgery (baseline), 24 hour, 48 hour, 72 hour, and day 7 post-surgery.)
  • Concentration of total free thiols(At study entry, before surgery (2 baselines), and once a day until day 7 after surgery, then at 14 and 21 days-post-surgery.)
  • Concentration of inflammatory derived-lipid mediators(Before surgery (baseline), 24 hour, 48 hour, 72 hour, and day 7 post-surgery.)
  • Concentration of nitrotyrosine(At study entry, before surgery (2 baselines), and once a day until day 7 after surgery, then at 14 and 21 days-post-surgery.)
  • Concentration of Ratio of F2-isoprostanes (F2-isop) and F2-isofurans (F2-isof)(At study entry, before surgery (2 baselines), and once a day until day 7 after surgery, then at 14 and 21 days-post-surgery.)

研究者

发起方
Coordinación de Investigación en Salud, Mexico
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Mariela Bernabe García

Full time researcher

Coordinación de Investigación en Salud, Mexico

研究点 (1)

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