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临床试验/NCT01845493
NCT01845493已完成1 期

Sulforaphane Supplementation in Atopic Asthmatics

University of North Carolina, Chapel Hill2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2013年4月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
16
试验地点
2
主要终点
mRNA levels of NRF2 and NRF2-dependent phase II enzymes in nasal epithelial cells

研究概览

简要总结

The investigators will perform a pilot study of daily treatment with oral sulforaphane (SFN) for 3 days to determine if Nuclear factor (erythroid-derived 2)-like 2 (NRF2) induction is possible with this supplementation regimen in individuals with allergic asthma.

详细描述

This pilot study will examine if oral SFN supplementation can induce NRF2 and NRF2-dependent phase II enzymes in nasal epithelial cells of allergic asthmatics. Subjects will receive both a SFN-rich broccosprout homogenate preparation and an alfalfa sprout homogenate (placebo) in a crossover fashion. mRNA levels of NRF2 and NRF2-dependent phase II enzymes will be compared between the active and placebo periods.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

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

入选标准

  • Age 18-50 of both genders
  • History of episodic wheezing, chest tightness, or shortness of breath after age of 6 years consistent with asthma, or physician diagnosed asthma after age of 6 years.
  • AND: Positive methacholine test. A positive test is defined as a provocative concentration of methacholine of 10 mg/ml or less producing a 20% fall in FEV1 (PC20 methacholine). Methacholine challenge in a separate screening protocol (98-0799), or from other venues will be accepted.
  • OR: Pre and post bronchodilator FEV1 improvement by 12% or more after 4 puffs of albuterol inhaler.
  • FEV1 of at least 80% of predicted and FEV1/FVC ratio of at least .70 (without use of bronchodilating medications for 12 hours), consistent with lung function of persons with no more than mild episodic or mild persistent asthma (NHANES III predicted set).
  • Allergic sensitization to at least one of the following allergen preparations: (House Dust Mite f, House dust mite p, Cockroach, Tree mix, Grass Mix, Weed Mix, Mold Mix 1, Mold Mix 2, Rat, Mouse, Guinea Pig, Rabbit, Cat or Dog) confirmed by positive immediate skin test response in a separate screening protocol. Proof of allergy from other venues, including ImmunoCAP testing from a medical workup, provided by the subject, will be accepted.
  • Oxygen saturation of > 94 % and normal blood pressure (Systolic between 150 - 90, Diastolic between 90-60 mm Hg)
  • Willing to provide information regarding health history and habits of cigarette smoke exposure;
  • Willing to avoid antioxidant vitamins and cruciferous vegetables as well as juices/drinks with added vitamin supplements for 2 days prior the baseline screening visit and throughout initial dosing period.
  • Subjects must be willing to avoid antihistamine use for 4 days prior to each session and NSAIDs for 7 days prior to each session. Nasal steroids must be held for 2 weeks prior to the session.

排除标准

  • Medical history or underlying health problems that preclude participation in the protocol per the study physician;
  • Current nutritional disorder such as anorexia, bulimia, irritable bowel syndrome, Crohn's disease etc;
  • Use of oral corticosteroids within the past 4 weeks;
  • Presence of upper or lower respiratory tract infection or treatment with antibiotics within the previous 4 weeks;
  • Pregnancy as determined by menstrual history or urine pregnancy test;
  • Current smokers will be excluded. Anyone with a smoking history > 0.5 pack year and/or >1 pack per month will also be excluded.
  • History of bleeding disorder;
  • Recent nasal surgery (with 6 months). If a subject has had nasal surgery between 6 months and 5 years, a study physician will visualize the area prior to the biopsy to evaluate the suitability of the nose for the procedure.
  • History of intolerance of or aversion to broccoli
  • Unable to withhold nasal steroids for 2 weeks before each session. These subjects may be deferred until after their allergy season.

结局指标

主要结局

mRNA levels of NRF2 and NRF2-dependent phase II enzymes in nasal epithelial cells

时间窗: 2 hours post third ingestion of SFN/placebo ingestion

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Michelle Hernandez, MD

Principle Investigator

University of North Carolina, Chapel Hill

研究点 (2)

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