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Ayurveda for Flu Like Illness During Covid-19 Outbreak

Not Applicable
Completed
Conditions
Flu Like Illness
Interventions
Dietary Supplement: Ayurveda
Other: Usual Care
Registration Number
NCT04351542
Lead Sponsor
Aarogyam UK
Brief Summary

This study aimed to evaluate the efficacy and safety of Ayurveda in reducing symptoms of flu like illness during the Covid 19 outbreak.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
Inclusion Criteria
  • Patients with fu like symptoms within 48 hours of onset during March2020
  • Mild to moderate symptoms who were advised to self isolate at home for 7-14 days
  • Flu like symptoms present at least one respiratory symptom (e.g. cough, nasal obstruction, sore throat) and at least one constitutional symptom other than fever (e.g. fatigue, headache, myalgias) of less than 48-hour duration
  • Willing to consent and follow up
Exclusion Criteria
  • Pregnant/lactating

    • Participants with chronic pulmonary diseases or critical condition or already developed severe respiratory distress
    • Clinically malignancies, systemic infection, other medical or psychiatric condition which places the subject at unacceptable risk to participate in the study - Known hypersensitivity to any ayurveda herbal substances
  • Severe symptoms of respiratory distress patients deemed to require intensive care immediately

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Ayurveda Care GroupAyurvedaIndividualised ayurveda treatment was given to participants based on individual constitution.
Usual Care GroupUsual CareParticipants followed the usual care.
Ayurveda Care GroupUsual CareIndividualised ayurveda treatment was given to participants based on individual constitution.
Primary Outcome Measures
NameTimeMethod
Severity of symptom scoreChange from baseline to 3rd and 7th day

Symptoms diary card completed twice daily from Day 0 to Day 7

Time to achieve afebrileChange from baseline to 3rd and 7th-day

Time to bring down a fever (oral temperature \< 37.2 ̊C)

Secondary Outcome Measures
NameTimeMethod
Patient reported improvementChange from baseline to 3rd and 7th-day

Patient reported improvement using 4 scale; 0-none, 1-weak, 2-medium, 3-strong

Trial Locations

Locations (1)

Aarogyam

🇬🇧

Leicester, United Kingdom

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