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临床试验/CTRI/2025/02/080248
CTRI/2025/02/080248尚未招募2 期

Efficacy & safety of a standardized extract from Bacopa monnieri in children & adolescents with attention deficit hyperactivity disorder (ADHD): A Randomized, Double-blind, Placebo-controlled with an extended open label clinical trial.

Natural Remedies1 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2025年2月19日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
136
试验地点
1
主要终点
ADHD symptoms as measured by the SNAP IV

研究概览

简要总结

Attention deficit and hyperactivity disorder  ADHD  is a common childhood disorder characterized by persistent symptoms of lack of attention  hyperactivity and impulsivity being associated to decreased school performance and academic success and social rejection  and in adults  it is related to worst performance and success in professional field

Children with ADHD have a significantly greater probability than their peers to develop conduct disorders during adolescence and personality disorders in adulthood

Ample number of resources are available in the public domain on the positive effectiveness of Bacopa**monnieriin improving attention  Also many literature suggest this plant extract may be effective in treating young patients with Attention deficit and hyperactivity disorder

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
6.00 Year(s) 至 16.00 Year(s)(—)
性别
All

入选标准

  • Children or adolescents of both sexes between 6 and 16 years old both inclusive who exhibit mild to moderate ADHD with predominantly inattentive or combined presentation according to DSM V criteria assessed via the MINI KID Inattentive subset and hyperactivity subset of not greater than 22 on SNAP IV scale Voluntary Assent to participate in the study from all those who are more than 7 years of age Informed Consent Form signed by legal guardians research participant when possible Results of laboratory tests chemistry blood count and urine physical examination and vital parameters with no clinically significant changes clinically significant changes are defined as laboratory results requiring acute drug intervention indicating severe illness or requiring further medical evaluation according to the discretion of the investigator.

排除标准

  • Wechsler Intelligence Scale for Children Fourth Edition Short Form WISC IV SF score subjects whose scores are less than 80 To be administered by a psychiatrist or a clinical psychologist Patients diagnosed with previous cognitive development delay Research participants with known hypersensitivity to the other medications History of alcohol or drug abuse by the research participant Where the immediate concern is around another Primary psychiatric diagnoses other than ADHD Diagnosis of psychiatric comorbidities except for simple phobia adjustment disorders learning disorders oppositional defiant disorder sleep disorders mild anxiety and or mild depressions History of seizures except for mild febrile seizures within 2 years from the time of recruitment Diagnosis of Tourette Syndrome and chronic tics Research participants who are making use of drugs for the treatment of ADHD in the last three months Research participants who are making use of anticonvulsants antidepressants and antipsychotics up to 6 weeks prior to study entry or during the same Positive beta HCG test for girls who have attained menarche Patients at identified risk of suicide through clinical interview Children or adolescents with ADHD predominantly hyperactive or impulsive Other conditions considered by the investigator as reasonable for disqualification of the subjects participation in the study.

结局指标

主要结局

ADHD symptoms as measured by the SNAP IV

时间窗: Timeframe on week 0 6 14 and 28 | Timeframe on week 0 6 14 and 28

CGI I Scale scores

时间窗: Timeframe on week 0 6 14 and 28 | Timeframe on week 0 6 14 and 28

次要结局

  • Computer based Continuous Performance Test scores

研究者

发起方
Natural Remedies
申办方类型
Pharmaceutical industry-Indian
责任方
Principal Investigator
主要研究者

Dr Ruchi Gupta

Pratyasha Mind Clinic

研究点 (1)

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