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Clinical Trials/CTRI/2023/07/055552
CTRI/2023/07/055552
Not yet recruiting
未知

An observational study to evaluate the correlation of doshik predominance in various stages of day night with kshaya vridhi in lakshanas of sandhivata amlapitta & Tamaka shwasa

Shri Krishna Govt Ayurvedic College and Hospital Kurukshetra Haryana0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: M199- Osteoarthritis, unspecified siteHealth Condition 2: K318- Other specified diseases of stomach and duodenumHealth Condition 3: J988- Other specified respiratory disorders
Sponsor
Shri Krishna Govt Ayurvedic College and Hospital Kurukshetra Haryana
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
Observational

Investigators

Sponsor
Shri Krishna Govt Ayurvedic College and Hospital Kurukshetra Haryana

Eligibility Criteria

Inclusion Criteria

  • 1\. Individuals between the age group of 20 to 70 years irrespective of the sex having clinical features of Sandhivata, Amlapitta and Tamaka shwasa as described in Ayurvedic Classics were selected.
  • 2\. Diagnosis of Sandhivata, Amlapitta and Tamaka shwasa will be purely decided only by considering the sign and symptoms mentioned in classics.
  • 3\. In Sandhivata radiology will not be carried out because patients who are already diagnosed radiologically are included in this study

Exclusion Criteria

  • 1\. Patients below 20 years and above 70 years.
  • 2\. Patients suffering from other forms of arthritis like RA, Psoriatic arthritis, gout, Ankylosis Spondylitis, infective arthritis and SLE
  • 3\. Patients already diagnosed with other systemic diseases such as nephropathic, neuropathic any type of malignant disorder, HTN, DM, Hypo/Hyper thyroidism, Cardiac asthma tropical pulmonary eosinophillia, acute and chronic Bronchitis, bronchiectasis, spontaneous pneumothorax, complicated Bronchial asthma, drug dependent cases and Pregnant women will be excluded from study

Outcomes

Primary Outcomes

Not specified

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