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Evaluation of nasal administration of extract of Brahmi leaves (INDCA-NS) in the treatment of tension-type headache

Phase 4
Conditions
Health Condition 1: G00-G99- Diseases of the nervous system
Registration Number
CTRI/2020/10/028285
Lead Sponsor
Indus Biotech Private Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

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.

Exclusion Criteria

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

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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