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Clinical evaluation of the effect on oral administration of Siddha classical drug VILVA ENNAI for the treatment of BRONCHIOLITIS.

Phase 2
Completed
Conditions
Acute bronchiolitis, unspecified,
Registration Number
CTRI/2021/01/030216
Lead Sponsor
Dr K Ragavi Sayi Saranya
Brief Summary

The study is a single arm clinical trial to evaluate the therapeutic efficacy of VILVA ENNAI for the treatment of VALI KANAM. The trial drug will be administered orally at the dose of 4 ml before the food once a day at morning for a period of 10 days in 56 patients. The trial period of 24 months will be carrying out in Government Siddha Medical College and Hospital, Palayamkottai, Tirunelveli, Tamilnadu.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
40
Inclusion Criteria
  • subjects with any of the following symptoms will be included in the study 1.
  • Fever associated with Respiratory symptoms, Urinary tract symptoms and Gastrointestinal symptoms 2.
  • Loss of appetite 3.
  • Vomitting 5.
  • Wheezing 6.
  • Decreased urine output 7.
  • Dryness of mouth 9.
  • Constipation.
Exclusion Criteria
  • Children below 3 years and above 12 years 2.
  • Fever due to malignancy, trauma, psychological factors 3.
  • High grade fever 4.
  • Cough with hemoptysis 5.
  • Fever associated with other complications such as HIV, meningitis, Tuberculosis 6.
  • Cardiac diseases 7.
  • Chronic Renal diseases 8.
  • Severe Dehydration.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Decreases the body temperature, cough, vomitting, constipation and other clinical symptoms.10 days
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Government siddha medical college and hospital, Palayamkottai

🇮🇳

Tirunelveli, TAMIL NADU, India

Government siddha medical college and hospital, Palayamkottai
🇮🇳Tirunelveli, TAMIL NADU, India
Dr K Ragavi Sayi Saranya
Principal investigator
8072252679
drsairagavi@gmail.com

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