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Clinical Trials/CTRI/2022/07/044280
CTRI/2022/07/044280
Not yet recruiting
Phase 2

A randomized comparative clinical study to evaluate the efficacy of Dhumapana (Ayurvedic fume inhalation therapy) and Bhutshuddhikriya (breathing technique) on pulmonary function and quality of life in healthy volunteers

Parul Ayurved Hospital0 sites0 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
Parul Ayurved Hospital
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Parul Ayurved Hospital

Eligibility Criteria

Inclusion Criteria

  • 1\.Healthy, Male or Female subjects between the age group of 18 years to 70 years (both inclusive).
  • 2\.Those who do not have any acute medical condition or chronic medical/surgical condition that requires either immediate or continuous medical monitoring or treatment.
  • 3\.Subjects who are ready to provide written informed consent and who are ready to willingly participate and follow the protocol requirements of the clinical study.

Exclusion Criteria

  • 1\. Pregnant and Lactating females
  • 2\. Known cases of Diabetes
  • 3\. Subjects having any medical or surgical condition that would require immediate medical or surgical intervention at the time of screening
  • 4\. Subjects having immune compromised status like HIV, Hepatitis, Tuberculosis and Cancer etc.
  • 5\. Subjects taking steroid treatment and or any kind of immunosuppressive therapy
  • 6\. Subjects participating in any other clinical study or having participated in any other study 3 months prior to screening in the present study.
  • 7\. Subjects having any addiction of smoking, alcohol.
  • 8\. Subjects doing Pranayama or any other breathing practice.
  • 9\. Other conditions, which in the opinion of the investigators make the patient unsuitable for enrolment or could interfere in adherence to of the study protocol

Outcomes

Primary Outcomes

Not specified

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