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临床试验/NCT04495816
NCT04495816已完成2 期

COVID-19 Anosmia Study

Icahn School of Medicine at Mount Sinai1 个研究点 分布在 1 个国家目标入组 139 人开始时间: 2020年7月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
139
试验地点
1
主要终点
Change in Brief Smell Identification Test (BSIT) in Participants With Laboratory-Confirmed COVID-19

研究概览

简要总结

To capture the natural history of COVID-19 associated olfactory dysfunction as measured by two patient reported outcome measures (SNOT-22, QOD-NS) and a 6-week BSIT with a comparison to an intervention arm receiving daily omega-3 supplements.

详细描述

Infection with the novel coronavirus (COVID-19) has been linked to new-onset olfactory dysfunction, often as the only presenting symptom. In one multicenter European study, 85.6% of patients with mild to moderate symptoms reported hyposmia or anosmia with early recovery of olfactory function in just under half of patients. However, the pathogenesis and natural history of COVID-19 related olfactory dysfunction is poorly understood.

Anosmia most commonly arises in association with sinonasal disease or post-infectious or post-traumatic disorders. Notably, olfactory loss has been associated with impaired quality of life, higher rates of depression, and even increased mortality risk. Spontaneous recovery has been observed in patients with post- infectious olfactory dysfunction, typically over a period of months to years, with an estimated one-third of patients demonstrating meaningful improvement after one year.

Smell retraining therapy appears to be an effective therapeutic option for patients with post-infectious olfactory dysfunction, particularly for patients who initiate treatment within one year from onset of symptoms, but requires an intervention period of at least three to four months. Various pharmacotherapies have been investigated in the treatment of post-infectious anosmia but none have clearly demonstrated utility with the exception of a possible benefit for nasal steroid irrigations in combination with smell retraining therapy.

More recently, omega-3 polyunsaturated fat supplementation has emerged as a promising pharmacotherapy for olfactory dysfunction in patients without sinonasal disease. Omega-3 fatty acid deficient mice demonstrate evidence of olfactory dysfunction and mice receiving omega-3 fatty acids have improved recovery after peripheral nerve injury, which has been linked to neuroprotective effects mediated through anti-oxidant and anti-inflammatory pathways. In humans, a large cross-sectional study found that older adults with higher dietary fat intake had lower incidence of olfactory impairment. From a clinical perspective, patients without sinonasal disease receiving postoperative omega-3 fatty acid supplementation after endoscopic endonasal skull base surgery in a randomized control trial demonstrated a significantly greater rate of return of normal olfactory dysfunction.

Little is known about either the natural history of olfactory dysfunction associated with COVID-19 infection or about the therapeutic efficacy of omega-3 fatty acid supplementation in patients with post-viral anosmia. The study team hopes to gain a better understanding of each through a randomized double-blind placebo control study that assesses both objective and subjective perception of olfactory dysfunction over a period of 6 weeks after infection.

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
Double (Participant, Investigator)

盲法说明

The healthcare providers interacting with the patients, as well as the participants themselves, will not know which arm they have been assigned to. Only the research fellows will have access to the randomization scheme.

入排标准

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

入选标准

  • Adults (18 years of age or older) with self-reported new-onset olfactory dysfunction
  • Positive COVID-19 diagnosis will be deemed eligible for inclusion.

排除标准

  • Patients <18 years of age
  • Patients who are unable to provide informed consent
  • Patients without a positive COVID-19 PCR result obtained through nasopharyngeal swab - Patients with a COVID-19 diagnosis but without self-reported anosmia
  • Patients with severe COVID-19 disease as defined by the Mouth Sinai Health System Treatment Guidelines for SARS-COV-2 (requiring high flow nasal cannula, non-rebreather, CPAP/BIPAP, or mechanical ventilation OR patients requiring pressor medication OR patients with evidence of end organ damage)
  • Patients with pre-existing self-reported olfactory dysfunction
  • Patients with a history of chronic nasal/sinus infections (rhinosinusitis) or history of endoscopic sinus surgery
  • Patients using nasal steroid sprays or irrigations for any reason
  • Patients who are prisoners of the state
  • Patients who have psychiatric or developmental disorder conditions that may impair ability to provide informed consent
  • Patients will also be excluded if they have an allergy to fish or an omega-3 supplement, or do not eat fish or fish- containing substances for any reason

研究组 & 干预措施

Omega-3

Active Comparator

1,000 mg of omega-3 fatty acid (2 softgels per day for 6 weeks)

干预措施: Omega-3 Fatty Acid Supplement (Drug)

Placebo/Control

Sham Comparator

2 softgels per day for 6 weeks

干预措施: Placebo/Control (Drug)

结局指标

主要结局

Change in Brief Smell Identification Test (BSIT) in Participants With Laboratory-Confirmed COVID-19

时间窗: Week 0 and Week 6

Mean change in BSIT in participants with severe olfactory dysfunction defined as BSIT ≤ 6. Brief Smell Identification Test (BSIT) is a 12-item instrument, full range score from 0 to 12, higher score indicates better olfactory performances.

Change in Brief Smell Identification Test (BSIT)

时间窗: Week 0 and Week 6

Change in BSIT. Brief Smell Identification Test (BSIT) is a 12-item instrument, full range score from 0 to 12, higher score indicates better olfactory performances.

Change in Brief Smell Identification Test (BSIT) in Participants With Severe Olfactory Dysfunction

时间窗: Week 0 and Week 6

Mean change in BSIT in participants with severe olfactory dysfunction defined as BSIT ≤ 7. Brief Smell Identification Test (BSIT) is a 12-item instrument, full range score from 0 to 12, higher score indicates better olfactory performances.

Change in Brief Smell Identification Test (BSIT) in Participants With Laboratory-Confirmed COVID-19 and Severe Olfactory Dysfunction

时间窗: Week 0 and Week 6

Mean change in BSIT in participants with laboratory-confirmed COVID-19. Brief Smell Identification Test (BSIT) is a 12-item instrument, full range score from 0 to 12, higher score indicates better olfactory performances.

次要结局

  • Sinonasal Outcomes Test (SNOT-22)(baseline, weeks 1, 2, 4 and 6 after softgel initiation)
  • Modified Brief Questionnaire of Olfactory Dysfunction (mQOD-NS)(baseline, weeks 1, 2, 4 and 6 after softgel initiation)

研究者

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

Alfred-Marc Iloreta

Assistant Professor

Icahn School of Medicine at Mount Sinai

研究点 (1)

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