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Clinical Trials/CTRI/2024/10/074674
CTRI/2024/10/074674Not yet recruitingNot Applicable

A Clinical Study on the Efficacy of Mahaswasari Loham in Tamaka Swasa with special reference to Bronchial Asthma

Dr Kummari Nikhitha1 site in 1 country30 target enrollmentStarted: October 14, 2024Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
To reduce the frequency of episodes of Shortness of breath

Study Overview

Brief Summary

Bronchial Asthma is a major non-communicable disease (NCD) & most common chronic obstructive lung disease affecting all age groups, which is characterized by chronic airway inflammation and increased airway hyper-responsiveness leading to symptoms of wheeze, cough, chest tightness and dyspnea.   It is characterized functionally by the presence of airflow obstruction which is variable over short periods of time or is reversible with treatment. Asthma is included in the WHO Global action plan for the Prevention and Control of NCDs and the United Nations 2030 Agenda for Sustainable Development and to make progress towards Universal Health coverage.  Bronchial Asthma is correlated with “Tamaka Swasa” based on the clinical features described in Ayurvedic Samhitas. â€œSwasati anena iti Swasah”(Shabda Kalpa Druma). In general, the word Swasa denotes respiration during physiological and pathologic conditions with normal and abnormal breathing pattern.***‘Tamaka swasa’***is one among the five types of SWASA ROGA, it is described as Vata Kaphaja vikara mainly originating from Pittasthana and then manifested through Pranavaha Srotas.  Due to nidanas (causative factors) Vata and Kapha gets prakopa in the Uras leading to vitiation of Pranavaha, Annavaha, Udakavaha srotas, later the obstructed Vayu travels in Pratiloma gati (reverse direction) and produces signs and symptoms of *Tamaka swasa.*During initial stages it is Sadhya (curable) and later it turns into Yapya vyadhi (palliable) if not treated properly.

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 65.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1.Who are willing to participate in the study and agree for the consent sign 2.symptoms exacerbations cough, wheeze, dyspnea greater than a week 3.Mild persistant cases of asthma of duration more than 6months 4.Night symptoms twice per month but less than twice per week 5.FEVI greater than 80% 6.spo2 greater than 92% 7.Non smokers.

Exclusion Criteria

  • 1.Moderate and severe persistent asthma 2.Asthma due to other systemic origin 3.suffering from diabetes,cardiac asthma, status asthmatics,CVDs, autoimmune disorders.
  • 4.HIV positive cases,pregnant women, lactating mothers 5.patients who need salbutamol inhaler daily 6.dyspnea due to other diseases like COPD, bronchiectasis, pulmonary tuberculosis, interstitial lung disease, occupational lung disease, malignancies.

Outcomes

Primary Outcomes

To reduce the frequency of episodes of Shortness of breath

Time Frame: 60 days

Secondary Outcomes

  • to reduce the signs and symptoms of bronchial Asthma(60 days)

Investigators

Sponsor
Dr Kummari Nikhitha
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Dr Kummari Nikhitha

Dr. BRKR Govt Ayurvedic college & Hospital

Study Sites (1)

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