Health Condition 1: J00- Acute nasopharyngitis [common cold]
Conditions
Interventions
Intervention1: Guduchyadi kwath syrup: Syrup comprising kwath made up of guduchi, nimba, dhaniya, shunthi, raktachandan, musta and madhu
Dose 1ml/kg body weight in 3 divided doses
Oral Route of admini
Sponsors
Dr Mahesh Narayan Gupta
Eligibility
Inclusion criteria
Inclusion criteria: Patients having allergic history. Patients who fulfill diagnostic criteria of Pratishyaya.
Exclusion criteria
Exclusion criteria: Patients below 2.00 years and above 10.00 years. Congenital defects and disorders. Patients having severe cardiovascular, gastrointestinal and renal disease. Hematological, neurological and psychiatric disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome will be assessed on the basis of improvement in the symptoms of Pratishyaya as cough, fever, post nasal discharge, nasal blockage, sneezing, nasal itching, running nose, headache, dryness of throat, pricking pain in temporal region, hoarseness of voice etc. The patients will be observed for both subjective and objective parameters (or as per requirement) on 7th day and 15th day during the trial. Another follow up will be done 15 days after completion of trial.Timepoint: The primary outcome will be assessed on the basis of improvement in the symptoms of Pratishyaya as cough, fever, post nasal discharge, nasal blockage, sneezing, nasal itching, running nose, headache, dryness of throat, pricking pain in temporal region, hoarseness of voice etc. The patients will be observed for both subjective and objective parameters (or as per requirement) on 7th day and 15th day during the trial. Another follow up will be done 15 days after completion of trial. | — |
Secondary
| Measure | Time frame |
|---|---|
| OBJECTIVE CRITERIA- The effect of medicine will also be analyzed on following parameters before and after treatment. â?¢ Hb%, TLC, DLC, ESR, AEC OVERALL EFFECT OF THERAPY- The total effect of therapy of this trial will be grouped as follow- 1. Complete remission - 100% 2. Markedly improvement - 75 -100% 3. Moderate improvement - 50 -75% 4. Mild improvement - 25 -50% 5. No improvement - 0 -25 %Timepoint: First follow up at 7th day and 2nd follow up at 15th day. OBJECTIVE CRITERIA- The effect of medicine will also be analyzed on following parameters before and after treatment. â?¢ Hb%, TLC, DLC, ESR, AEC OVERALL EFFECT OF THERAPY- The total effect of therapy of this trial will be grouped as follow- 1. Complete remission - 100% 2. Markedly improvement - 75 -100% 3. Moderate improvement - 50 -75% 4. Mild improvement - 25 -50% 5. No improvement - 0 -25 % | — |
Countries
India
Contacts
Public ContactDr Sneha Tripathi
State Ayurvedic College, Lucknow
Outcome results
None listed