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Role of Guduchyadi Ghrita in the management of the Mild Neurocognitive Disorder.

Phase 3
Conditions
Health Condition 1: G318- Other specified degenerative diseases of nervous system
Registration Number
CTRI/2023/04/051695
Lead Sponsor
Institute of Teaching and Research in Ayurveda
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1) Subjects irrespective of gender, fulfilling the criteria of Mild Neurocognitive Disorder as per DSM V.

2) Age group â?? 40 - 70 years

3) Montreal Cognitive Assessment scale [MoCA] (18 to 25)

4) Patients willing to accept participation in the clinical trial.

Exclusion Criteria

1) Age below 40 years and above 70 years.

2) Subjects with major depression or other psychiatric disorders or currently undergoing treatment for depression.

3) Use of psychoactive medication that would affect the subjectâ??s ability to reliably perform on neurocognitive testing.

4) Subjects with Malignant disease, HIV or serious infection.

5) Subjects with Cardiovascular, Renal or Hepatic disorder, Thyroid dysfunction.

6)subjects with Stage II HTN or above (Blood Pressure >160/100 mm of Hg), Diabetes (FBS >200 mg/dl), Dyslipidemia (Severe Hypertriglyceridemia,TG >500 mg/dl and /or, LDL >190 mg/dl)

7) Subjects who have decline in cognitive functions as a result of surgery and trauma.

8) Visual/auditory impairment that would preclude the participant from participating in or cooperating with the protocol.

9) Pregnant women and lactating mothers.

10) Patient with alcohol abuse.

11) Subjects who are not able to read, write and comprehend Hindi language properly for comprehending the assessment tests.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement in cognitionTimepoint: At baseline ,4th week , 8th week , 10th week , 12 th week
Secondary Outcome Measures
NameTimeMethod
Improvement of quality of life of the patients with mild Neurocognitive DisorderTimepoint: Baseline and 8th week
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