CTRI/2018/02/011918
Not yet recruiting
Phase 3
A Comparative study to Evaluate Efficacy of Shwasa Kuthar Rasa and Pippali Vardhman Rasayan in the management of Chronic Obstructive Pulmonary Disease(Praanavaha Sroto Dushti) - COPD
Ch Brahm Prakash Ayurved Charak Sansthan0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- Patients of COPD
- Sponsor
- Ch Brahm Prakash Ayurved Charak Sansthan
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Age Group between 35\-65 years.
- •2\. Patients of Both Sexes.
- •3\. Smoking history current or former active ciggarette smokers or history of occupational exposure to COPD.
- •4\.Patients present with signs and symptoms of COPD.
- •5\.Radiographic evidence suggestive of COPD.
- •6\.Spiro\-metric diagnosis of COPD(as per GOLD criteria)
- •7\. The patients who are ready to sign informed consent form to participate in study.
- •8\. The patients who are ready to be consistent in visits during whole trial period.
- •9\. Firm home address and contact number which is readily accessible during whole course of trial.
Exclusion Criteria
- •1\)Seriously ill and morbid patients which are unlikely to survive for next 6 months.
- •2\)Pregnant and lactating women
- •3\)Patient with alcohol dependence
- •4\)History of hypersensitivity to any of trial drug
- •5\)Patient with serious hepatic disorder, renal disorder, diabetes mellitus or any condition that may jeopardize the study
- •6\)Patient with any other concomitant respiratory disorder
- •7\)Patient with co\-morbid disorders(Diabetes Mellitus, Pulmonary Tuberculosis ,Rheumatoid Arthritis , Carcinoma)
- •8\)Patient with poorly controlled hypertension (systolic \>160 mmHg and diastolic \> 100 mmHg)
- •9\) Patient receiving mast cell stabilizers, anti\-depressants, anticholinergics etc. or any other drugs that may have an influence on the outcome of the study.
Outcomes
Primary Outcomes
Not specified
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