SARS-COV-2. SARS-associated coronavirus as the cause of diseases classified elsewhere
Conditions
Interventions
Single intervention group. Methods: 34 COVID-19 patients (males and females) with mild to severe symptoms were given the Intervention. Baseline treatment
1gm of PAK-20 in 250ml of Combo 1 (soup/meat stock) twice a day for a max of 12 days, 50 ml of Oniater (onion water) once a day for 3 days. Hing (Asafoetida) tempering added to daily food diet to add
Combo 2 (herbal tea), 250ml of twice a day for a maximum of 12 days. Datseed (date filled with black seeds, once a day for a maximum of 12 days. Use of protein heavy diets, fruits, milk shakes and fre
Sponsors
Knowledge Research and Innovation Center, Pakistan (KRIC)
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Both genders Aged between 18-80 years Mild, moderate or severe infection COVID-19 positive on the basis of symptoms, physical test and lab test
Exclusion criteria
Exclusion criteria: Any tumor or malignancy Recent surgery Patient on invasive / non-invasive ventilator (critical) Taking any other medicine parallel to PAK-20, Oniater and Hing for treatment of COVID-19. Taking any immunosuppressant
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fever. Timepoint: Before intervention and (1,3,5) odd days after intervention. Method of measurement: Thermometer.;Cough. Timepoint: Before intervention and (1,3,5,7,9,11) odd days after intervention. Method of measurement: Cough Scale.;Sore Throat. Timepoint: Before intervention and (1,3,5,7,9,11) odd days after intervention. Method of measurement: Sore Throat Scale.;Shortness of Breath. Timepoint: Before intervention and (1,3,5,7,9,11) odd days after intervention. Method of measurement: Borg Scale of Short of Breath.;Muscle Pain. Timepoint: Before intervention and (1,3,5,7,9,11) odd days after intervention. Method of measurement: Numeric pain rating Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| PCR-RT for COVID-19. Timepoint: Before intervention and 14th day after intervention. Method of measurement: PCR-RT Lab test.;Chest X-ray. Timepoint: Before intervention and on 14th day after intervention. Method of measurement: Radiological X-ray findings.;10 Second Breath Hold Test. Timepoint: Before intervention and on 14th day after intervention. Method of measurement: Physical 10 Second breath Hold. | — |
Countries
Pakistan
Contacts
Public ContactUmber Nawaz
Knowledge Research and Innovation Center, Pakistan (KRIC)
Outcome results
None listed