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A randomised open label study on potential effects of Ayurveda in schizophrenia

Phase 3
Conditions
Health Condition 1: F20- Schizophrenia
Registration Number
CTRI/2023/08/056921
Lead Sponsor
DrAkhila Soman
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Diagnosed patients of Unmada according to Ayurveda and patients of Schizophrenia as per DSM-5-TR

Patients with predominant Negative symptoms (Any of the 4 Global scores of

Scale for the Assessment of Negative Symptoms- SANS= 3).

Mild or lesser level of positive symptoms (Global score of all items of Scale for

the Assessment of Positive Symptoms SAPS < 3)

Patients who are in the capacity to provide informed consent (as assessed by

UBACC- University of California, San Diego Brief Assessment of Capacity to

Consent (UBACC) will be recruited. Those who do not have the capacity, caregiver’s consent will be

taken.

Patients who are on stable medications for atleast 1 month.

Exclusion Criteria

Patients with bipolar affective disorder, substance use disorders (except

nicotine and caffeine), major systemic illness, neurological disorders and

immune system disorders.

Patients with suicidal tendencies.

Patients scoring > 7 in Hamilton Depression Rating Scale.

Pregnant and lactating mothers.

Patients unsuitable for Vamana procedure – heart diseases, severe hepatic,

renal or pulmonary dysfunction.

Patients who have undergone Vamana or Virechana karma in the last 3

months.

Study & Design

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