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临床试验/CTRI/2019/05/019431
CTRI/2019/05/019431已完成不适用

A Randomized, Double Blind, Placebo Controlled Interventional Clinical Study to evaluate the efficacy and safety of Investigational Product SLEPOVIN in patients with Insomnia

BigBrother Nutra Care Pvt Ltd1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2019年5月30日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
•Mean change in Subjective Sleep Efficiency (sSE)

研究概览

简要总结

Sleep disorders are a common ailment in currentsociety, one that has significant implications for public health1. Insomnia,the most common of those sleep disorders, is defined by the Diagnostic andStatistical Manual of Mental Disorders, Fourth Edition as difficultyinitiating sleep, difficulty maintaining sleep, or difficulty obtainingrestorative sleep with associated daytime dysfunction or distress due to thatlack of sleep2. It is associated with significant health problemsincluding reduced quality of life, work productivity, and mental health.Insomnia has a high prevalence in society; and although numbers vary,approximately two thirds of adults will have one or more episodes of insomniaeach year, and approximately 15% of adults per year will have a serious chronicepisode3. Insomnia is the most common sleep disorder affectingmillions of people as either a primary or comorbid condition4.Insomnia has been considered as both a symptom and a disorder, and thisdistinction may affect its conceptualization from both research and clinical perspectives.Thecurrent therapeutic options in Insomnia patients include pharmacological,psychological, and complementary approaches. Pharmacologic medications includebenzodiazepine hypnotics, non-benzodiazepine, and melatonin receptor agonists.  Due to associated adverse events withpharmacologic treatments, insomnia patients are switching to alternativetherapy such as herbal medications, alternative therapy encompasses a varietyof disciplines that include everything from diet and exercise to mental conditioningand lifestyle changes such as acupuncture, guided imagery, yoga, hypnosis, biofeedback, aromatherapy, relaxation, herbalremedies, massage, and many others.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Male or female subjects aged above 18 years old (inclusive)
  • Subject is in good physical status and mental health
  • Male or female subjects aged above 18 years old (inclusive) 4.Subject is in good physical status and mental health
  • Sleep onset insomnia (difficulty taking sleep at the beginning of the night)
  • Sleep maintenance insomnia (difficulty in maintaining the sleep)
  • Nocturnal awakenings, difficulty in retuning to sleep after awakening in the middle of the night or wakening early in the morning
  • Insomnia severity index > 7
  • Subject is willing to limit alcohol, caffeine, and nicotine consumption while in the study
  • Habitual bedtime between 8.30 pm and midnight
  • Able and willing to follow all study related instructions and to complete all required visits
  • Subjects willing to give inform consent for participation.

排除标准

  • Subjects with clinically significant endocrine, metabolic, hepatic, renal, cardiovascular, gastrointestinal, respiratory, hematological or neurological illness (es)
  • History of bipolar disorder, psychotic disorder, or posttraumatic stress disorder, or current psychiatric disorder that requires a prohibited medication
  • Subjects who suffer from sleep disorder other than primary insomnia including restless leg syndrome and sleep apnea
  • Subjects with substance dependence/ abuse in the past one year or with alcohol abuse are ineligible
  • Subjects taking certain prohibited medications
  • Females who are pregnant, lactating or likely to become pregnant during the study
  • Subjects using tobacco products or caffeinated beverages during night awakenings.
  • Clinical history of allergy/ hypersensitivity to one or more products of herbal origin.
  • Is currently participating or has participated in another interventional clinical study at this or any other facility in the past 3 month.

结局指标

主要结局

•Mean change in Subjective Sleep Efficiency (sSE)

时间窗: Day 0 Day 30

•Mean change in sSOL, sWASO, and Subjective Total Sleep Time (sTST)

时间窗: Day 0 Day 30

•Mean change in Subjective Sleep Onset Latency (sSOL) (Time frame: Beginning of placebo-controlled treatment 1 month of placebo-controlled treatment.

时间窗: Day 0 Day 30

次要结局

  • •Change in Insomnia Severity Index from baseline to end of visit(•Changes in Epworth Sleepiness Scale from baseline to end of visit)

研究者

发起方
BigBrother Nutra Care Pvt Ltd
申办方类型
Pharmaceutical industry-Indian

研究点 (1)

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