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临床试验/CTRI/2020/10/028285
CTRI/2020/10/028285尚未招募4 期

Evaluation of efficacy and safety of intranasal administration of standardized extract of Centella asiatica leaves (INDCA-NS) in the treatment of subjects with tension-type headache: A prospective, randomised, double-blind, placebo-controlled, multicenter, interventional, parallel study.

Indus Biotech Private Limited0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1.Male and female subjects aged 18 years and above.
  • 2.Subjects experiencing episodic tension type headaches which satisfy the following criteria: At least 10 episodes of headache, occurring on < 1 day per month on average ( <12 days per year) (Infrequent Tension Type Headache) or occurring 1 to 14 days per month on average for 3 months (>=12 days per year to < 180 days per year) (Frequent Tension Type Headache) and the subject satisfies inclusion criteria 3 through 6.
  • 3.Headache lasting from 30 minutes to seven days.
  • 4.A headache has at least two of the following four characteristics; (i) bilateral location, (ii) pressing or tightening (non-pulsating) quality, (iii) mild or moderate intensity, (iv) not aggravated by routine physical activity such as walking or climbing stairs.
  • 5.Both of the following (i) no nausea or vomiting, and (ii) no more than one of photophobia or phonophobia.
  • 6.Not better accounted for any other ICHD-3 diagnosis.
  • 7.Subjects who are experiencing mild to moderate stress; stress score >=15 to <= 25 as per 21 item Depression, Anxiety, Stress Scale (DASS-21) at screening.
  • 8.Subjects who can understand and complete the subject oriented English language questionnaires
  • 9.Providing informed written consent.

排除标准

  • 1.Pregnant, planning to become pregnant or breastfeeding women.
  • 2.Menopausal women experiencing headaches as part of the Menopause Syndrome
  • 3.Secondary headache to other causes (subarachnoid haemorrhage, cerebral haemorrhage, cerebral embolism, cerebral thrombosis, vascular malformation, arthritis, hypertension, or arteriosclerosis)
  • 4.Current or past history of a serious illness including, seizures, major psychiatric illness, structural brain disease, liver or kidney failure, organ transplantation, rheumatoid arthritis, uncontrolled hypertension, uncontrolled diabetes or malignancy
  • 5.Alcohol or substance abuse
  • 6.Use of anti-psychotics, serotonergic, antidepressants or benzodiazepines, and other medications that could cause serotonin syndrome for example St Johns Wort and Tramadol in the four weeks prior to commencing the study.
  • 7.Allergy or sensitivity to any of the ingredients in the study treatment

研究者

发起方
Indus Biotech Private Limited

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