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Safety and Efficacy of Urtica Dioica Cataplasm in the Management of Osgood-Schlatter Disease in Young Athletes

F

Faculty of Medicine, Sousse

Status

Not yet enrolling

Conditions

Osgood-Schlatter Disease

Treatments

Other: Urtica dioica cataplasm
Drug: Vitamin D
Other: Placebo
Behavioral: Resting conditions

Study type

Interventional

Funder types

Other

Identifiers

NCT07096037
UDC-OSD-2025

Details and patient eligibility

About

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:

  • UDC Group: topical application of Urtica dioica cataplasm
  • Standard Care Group: oral vitamin D supplementation and physical rest
  • Placebo Group: topical application of a placebo cataplasm using Beta vulgaris subsp. cicla

Enrollment

90 estimated patients

Sex

Male

Ages

7 to 15 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Healthy male children between 7 and 15 years of age
  • Active in regular sports practice (e.g., football)
  • Clinically confirmed diagnosis of OSD

Exclusion criteria

  • Known allergy to Urtica dioica
  • Presence of dermatological conditions or lesions on the knees
  • Recent use of anti-inflammatory medications
  • History of immune or chronic inflammatory diseases
  • Diagnosis of any other bone disorder

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

90 participants in 3 patient groups, including a placebo group

Urtica dioica cataplasm
Experimental group
Description:
Topical application of Urtica dioica cataplasm
Treatment:
Other: Urtica dioica cataplasm
Standard Care Group
Active Comparator group
Description:
Oral vitamin D supplementation and physical rest
Treatment:
Behavioral: Resting conditions
Drug: Vitamin D
Placebo
Placebo Comparator group
Description:
Topical application of a placebo cataplasm
Treatment:
Other: Placebo

Trial contacts and locations

0

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Central trial contact

Hana Nasrallah, PhD; Amira Zairi, Pr.

Data sourced from clinicaltrials.gov

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