Skip to content

To check the effectiveness of Ginger Jaggery electuary in management of COPD.

Clinical study to evaluate effectiveness of Guda-Ardrak Kalpa in management of Pranvaha Stroto Dushti

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023255
Enrollment
60
Registered
2020-02-11
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: J449- Chronic obstructive pulmonary disease, unspecified

Interventions

Intervention1: GUDA ARDRAK KALPA: 12gm Guda Ardrak Kalpa (6gm Guda and 6gm Ardraka) on day 1 along with 100ml of milk during 7.00-8.00 am is given. Subsequently 12gm Guda Ardrak and 50ml of milk is in

Sponsors

CH BRAHM PRAKASH AYURVED CHARAK SANSTHAN
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients having clinical features of Pranvaha stroto dushti. 2. Clinical symptoms of COPD described in GOLD 2019 report. 3. Patients suffering from Chronic Bronchitis. 4. Patients who are ready to give consent for trial with firm residential address and contact number

Exclusion criteria

Exclusion criteria: 1. Any surgery in abdomen, chest or eye in last 3 years. 2. Pregnancy and Lactation. 3. Any episode of MI in last 3 months. 4. Currently taking treatment for TB. 5. Hospitalized in last 3 months due to any heart problem and poorly controlled hypertension. 6. Subjects having tachycardia at rest. 7. Seriously ill and morbid patients. 8. Hypersensitivity to either Ginger or Jaggery. 9. Patients receiving anti depressants, mast cell stabilizers, or any other drug that may influence the outcome of study. 10. Patients diagnosed with type 1 and type 2 Diabetes

Design outcomes

Primary

MeasureTime frame
Reduction in SGRQ(St. George Respiratory Questionnaire) ScoreTimepoint: Day 1 Day 6 Day 12 Day 18 Day 24 Day 30 Day 36

Secondary

MeasureTime frame
BDI-TDI ScoreTimepoint: Day 1 Day 36;Improvement in severity of symptomsTimepoint: Day 1 Day 36;Reduction in frequency of need for emergency medicationTimepoint: Day 1 Day 36;Status of PrakrutisthapanaTimepoint: Day 1 Day 6 Day 12 Day 18 Day 24 Day 30 Day 36;TLC CRP ESR Sr. Uric AcidTimepoint: Day 1 Day 36

Countries

India

Contacts

Public ContactDr YOGESH KUMAR PANDEY

Ch. Brahm Prakash Ayurved Charak Sansthan

drishyadinesh@gmail.com9717226093

Outcome results

None listed

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