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Clinical Trial to evaluate the effectiveness of siddha formulation Thirikadugu Dravagam in the management of Swasakaasam

An Open Clinical trial to Clinical Trial to evaluate the effectiveness of siddha formulation Thirikadugu Dravagam in the management of Swasakaasam (Bronchial Asthma) among patients reporting at Ayothidoss Pandithar Hospital,National Institute of Siddha. - nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084371
Enrollment
30
Registered
2025-04-08
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: J454- Moderate persistent asthma

Interventions

Intervention1: Thirikadugu Dravagam: 5 ml bds with luke warm water ,oral route for 48 days Control Intervention1: Not applicable: Not applicable

Sponsors

National Institute of Siddha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients who are willing to undergo a Pulmonary function test (FEV1 between 50% - 80%) will be included. 2.Patients with any 2 or more of the following clinical symptoms will be included: H/O Wheezing minimum 2 episodes per week Cough with or without expectoration Dyspnea Tightness of chest 3.Patients who are willing to undergo radiological investigations and provide blood samples for lab investigations.

Exclusion criteria

Exclusion criteria: K/H/O Restrictive Lung diseases K/H/O Tuberculosis K/H/O Emphysema K/H/O Pleural effusion K/H/O Pneumothorax K/H/O Cardiac diseases K/H/O Renal diseases

Design outcomes

Primary

MeasureTime frame
Primary Outcome is assessed by comparing the improvement in the clinical signs and symptoms by Asthma Control Test (ACT) before and after treatment.Timepoint: 48 days

Secondary

MeasureTime frame
Changes in laboratory parameters of CBC, IgE, and Absolute Eosinophil Count (AEC) before and after treatment and improved lung volumes and capacities using Pulmonary Function Tests before and after treatment.Timepoint: 48 days

Countries

India

Contacts

Public ContactDr T LAKSHMIKANTHAM

National Institute of Siddha

drlakshmiramaswamy@gmail.com9025575185

Outcome results

None listed

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