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To study the efficacy of Ashwagandhadi Avaleha as an Adjuvant with Anti Tubercular Treatment.

A Pre-clinical and Clinical Study to evaluate the efficacy of Ashwagandhadi Avaleha as an Adjuvant in the management of Tuberculosis with Anti Tubercular Treatment.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033863
Enrollment
60
Registered
2021-05-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J989- Respiratory disorder, unspecified

Interventions

Intervention1: Ashwagandhadi Avaleha: Ashwagandhadi Avaleha 10gm BD along with Anti Tubercular Treatment (HRZE) for 8 weeks(intensive phase of ATT regimen) Control Intervention1: HRZE(Isoniazid, Ri

Sponsors

Principal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Freshly diagnosed cases of tuberculosis(Pulmonary Tuberculosis and Tubercular pleural effusion) 2. Patients of either sex between the age of 15-70 years. 3. Patients willing and able to participate for 8 weeks duration

Exclusion criteria

Exclusion criteria: 1. MDR and XDR cases of tuberculosis. 2. Patients having diabetes mellitus. 3. Patient with uncontrolled hypertension. 4. Suffering from any other chronic infections including HIV. 5. Patients Below the age of 15yrs and above the age of 70yrs. 6. Patients not willing for trial. 7. Individuals who have completed participation in any other clinical trial during the past three months. 8. Any other condition which the Principal investigator thinks may jeopardize the study.

Design outcomes

Primary

MeasureTime frame
Efficacy of Ashwagandhadi Avaleha to reduce/prevent toxicity when administered as add on therapy along with Anti tubercular drugs in the management of TuberculosisTimepoint: 8 weeks

Secondary

MeasureTime frame
Efficacy of the Ashwagandhadi Avaleha in improving general well being.Timepoint: 8 weeks

Countries

India

Contacts

Public ContactDr Pratibha Thakur

RGGPG Ayurvedic College and Hospital , Paprola

dranjana269@gmail.com9418312324

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026