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临床试验/NCT02012790
NCT02012790已完成不适用

Clinical & Metabolic Effects of Altering n-3 & n-6 Fatty Acids in Migraine (RCT)

University of North Carolina, Chapel Hill2 个研究点 分布在 1 个国家目标入组 182 人开始时间: 2014年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
182
试验地点
2
主要终点
Primary metabolic outcome: 17-hydroxy docosahexaenoic acid (DHA)

研究概览

简要总结

Migraine is a widespread, debilitating, chronic pain disorder and a major public health challenge. Most conventional, pharmaceutical treatments fail to give satisfactory long-term relief and their repeated use can have important side effects. This project involves implementation of substantial dietary changes in adults with migraine. Our goal is to test the hypothesis that a causal relationship exists between migraine symptoms and the amount and proportions of foods consumed containing defined amounts of polyunsaturated fatty acids.

Significant findings supporting the hypothesis will lead to a major shift in both prevention and management of migraine and other chronic pain disorders. Emphasis is on low-cost, health improvement strategies utilizing specific dietary modifications for pain management, based on solid clinical research evidence.

详细描述

Episodic migraine is a debilitating chronic pain condition afflicting 12% of American adults. Current conventional treatments rely on medications that provide limited or transient relief, target symptoms rather than the underlying causes of pain, and are associated with significant side effects and costs. It is therefore essential to investigate non-pharmacologic approaches to conventional headache treatments. Certain fatty acids and their bioactive metabolites regulate multiple pain-related biochemical pathways. Controlled clinical trials investigating pain modulation in response to dietary changes while exploring relevant mechanisms of action in humans are lacking.

In a recent feasibility study in patients with chronic daily headache (CDH), we found that targeted fatty acid modifications altered circulating endovanilloids, while reducing headache frequency and improving quality of life. These findings support our proposed model in which diet-induced alterations in endovanilloids modulate transient receptor potential cation channel subfamily V member 1 (TRPV1) activity in vivo, leading to important implications for migraine and chronic pain in general.

The goal of this research is to assess whether dietary PUFA modifications can result in predicted changes in circulating endovanilloids and improvement in headache-related clinical outcomes. The proposed 3-arm, 26-week,randomized, controlled, single-blind trial, with 51 subjects in each group, includes a 4-week baseline of usual care, followed by randomization to one of three 22-week dietary interventions plus usual care. Each of the three arms involves specific modifications of dietary fatty acid intakes through a whole foods diet. Participants in the dietary interventions receive food sufficient for 2 meals and 2 snacks daily along with extensive dietary counseling.

Specific aims are:

  1. To assess the efficacy of the dietary interventions in inducing the predicted changes in circulating fatty acid endovanilloid derivatives;
  2. To compare the clinical effects in migraine specific outcomes of two 16-week analgesic dietary interventions with each other and a control diet;
  3. To test, in an exploratory manner, our model of the proposed causal chain linking changes in fatty acids, their endovanilloid derivatives, and headache clinical endpoints.

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
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 years of age or older
  • Either gender
  • Meets 2004 International Classification of Headache Disorders-II* criteria for Episodic Migraine
  • Frequent migraine headaches
  • Headache history: > 2 years leading up to study meeting migraine criteria
  • Willing to complete daily diary for 26 weeks
  • Able to attend 8 dietitian counseling sessions
  • Under care of a physician for headaches
  • Able to read and communicate in English

排除标准

  • Marked depression, anxiety or psychosis.
  • History of specific food allergies, such as, but not limited to, dairy or gluten products
  • Pregnancy or anticipated pregnancy
  • Active treatment for a major medical illness, such as malignancy, autoimmune, immune deficiency disorder, etc.
  • History of significant head trauma or head/neck surgery within the past 3 years
  • History of subarachnoid or intra-cerebral hemorrhage or subdural hematoma
  • Allergy to fish or strong aversion to fish consumption.
  • History of nervous system infection such as meningitis or encephalitis within the preceding 5 years
  • History of vasculitis, intracranial mass, clotting disorder
  • Cognitive dysfunction that would prevent informed consent

结局指标

主要结局

Primary metabolic outcome: 17-hydroxy docosahexaenoic acid (DHA)

时间窗: Change in 17-hydroxy DHA at 16 weeks

17-hydroxy DHA is the pathway marker and precursor to two families of potent bioactive mediators with analgesic properties (D series resolvins and protectins), which will be measured at baseline and after 16 weeks of diet exposure.

Primary clinical outcome: Headache-specific Quality of Life (HIT-6)

时间窗: Change in HIT-6 at 16 weeks

The HIT-6 is a validated questionnaire designed "to measure the impact that headaches have on the ability to function on the job, at school, at home, and in social situations"

次要结局

  • Headache hours per day (headache frequency) are measured by a daily Headache Diary(Trajectory of change: -4 to 0 weeks (pre-intervention), 0-16 weeks (intervention), and 16-22 weeks (post-intervention))
  • Patient-Reported Outcomes Measurement Information System-29 Profile(Pre-post and trajectory of change measured at randomization and at 4,10, and 16 weeks after randomization)
  • 17-hydroxy DHA trajectory(Trajectory of change in 17-hydroxy DHA 0-16 weeks and 16-22 weeks)
  • HIT-6(Trajectory of change pre-intervention, 0-16 weeks, and 16-22 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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