This waitlist-controlled trial aims to evaluate the therapeutic effectiveness of Hayfever Care by assessing disease-specific symptoms over a 4-week period. Additionally, the study examines the tolerability and safety of the solution.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
63
Powdered natural food supplement provided as a decoction, to be taken twice daily. Personalized Diet and Nutrition Guidance along with Lifestyle Advice
Personalized Diet and Lifestyle Advice
Gyansanjeevani India
Jaipur, Rajasthan, India
Well-being Numerical Rating Scales
Time frame: Change from Baseline to 4 weeks after baseline
Change of Symptom Dry Eyes
Time frame: Change in symptom scores from baseline to 4 weeks.
Change of Symptom Itching Eyes
Time frame: Change in symptom scores from baseline to 4 weeks.
Change of Symptom Burning Eyes
Time frame: Change in symptom scores from baseline to 4 weeks.
Change of Symptom Respiratory Complaints
Time frame: Change in symptom scores from baseline to 4 weeks.
Change of Symptom Sneezing
Time frame: Change in symptom scores from baseline to 4 weeks.
Change of Symptom Rhinitis
Time frame: Change in symptom scores from baseline to 4 weeks.
Change of Symptom Fatigue
Time frame: Change in symptom scores from baseline to 4 weeks.
Change of Symptom Headache
Time frame: Change in symptom scores from baseline to 4 weeks.
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