CTRI/2022/04/041912Not yet recruitingNot Applicable
Development of scale for the assessment of strength of Satva and to evaluate its influence on RÄjayaká¹£mÄ with special reference to Pulmonary Tuberculosis
Institute of Medical Science Banaras Hindu University Varanasi Uttar Pradesh India1 site in 1 country75 target enrollmentStarted: April 25, 2022Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 75
- Locations
- 1
- Primary Endpoint
- To evaluate the type of Satva and its role in response to the treatment of Pulmonary Tuberculosis.
Study Overview
Brief Summary
This study is a single group prospective observational study to evaluate the strength of satva and its role in Pulmonary Tuberculosis. The primary outcome will association of the type of Satva and its role in response to the treatment of Pulmonary Tuberculosis. The secondary outcome will be the association of types of Satva with adverse reactions and complications of Pulmonary Tuberculosis.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18.00 Year(s) to 70.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •1.Confirmed pulmonary tuberculosis patients irrespective of gender 2.Patients with well controlled comorbid conditions 3.Age group between 18-70 years.
Exclusion Criteria
- •1.Not willing to complete the consent process as describe in proforma.
- •2.Inability to comply with study procedures and methods.
- •3.HIV patients.
Outcomes
Primary Outcomes
To evaluate the type of Satva and its role in response to the treatment of Pulmonary Tuberculosis.
Time Frame: 1.5yr
Secondary Outcomes
- To evaluate the association of types of Satva with adverse reactions and complications of Pulmonary Tuberculosis.(1.5 yr)
Investigators
Study Sites (1)
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