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The primary objective of this clinical trial is to evaluate the efficacy and safety of a topical Urtica dioica cataplasm in managing knee pain and functional limitations in athletic children diagnosed with Osgood-Schlatter Disease. Efficacy will be assessed through changes in knee pain using the Visual Analog Scale (VAS) and functional outcomes using the Knee Injury and Osteoarthritis Outcome Score (KOOS). Three groups will be tested:
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90 participants in 3 patient groups, including a placebo group
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Hana Nasrallah, PhD; Amira Zairi, Pr.
Data sourced from clinicaltrials.gov
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